| 1 | Straightforward, scalable, solution-phase synthesis of peptide bonds in flow | 1.7 | 0 | Citations (PDF) |
| 2 | Automated multistep synthesis of 2-pyrazolines in continuous flow | 2.8 | 3 | Citations (PDF) |
| 3 | Photoredox‐Catalyzed Preparation of Sulfones Using Bis‐Piperidine Sulfur Dioxide – An Underutilized Reagent for SO2 Transfer | 3.4 | 4 | Citations (PDF) |
| 4 | Nitro-sulfinate Reductive Coupling to Access (Hetero)aryl Sulfonamides | 3.5 | 8 | Citations (PDF) |
| 5 | Antascomicin B stabilizes FKBP51-Akt1 complexes as a molecular glue | 2.0 | 10 | Citations (PDF) |
| 6 | Palladium catalysts supported on biodegradable urea-based polymers in synthesis with CO – Part B | 4.7 | 5 | Citations (PDF) |
| 7 | Carbonylative transformations with Pd catalysts supported on bio-degradable urea-based polymer – Part A | 4.7 | 2 | Citations (PDF) |
| 8 | Exploring the chemical space of phenyl sulfide oxidation by automated optimization | 2.8 | 12 | Citations (PDF) |
| 9 | Automated multi-objective reaction optimisation: which algorithm should I use? | 2.8 | 46 | Citations (PDF) |
| 10 | Multicomponent Direct Assembly of N-Heterospirocycles Facilitated by Visible-Light-Driven Photocatalysis | 3.5 | 9 | Citations (PDF) |
| 11 | CLICK-enabled analogues reveal pregnenolone interactomes in cancer and immune cells | 3.5 | 12 | Citations (PDF) |
| 12 | Formation and utility of reactive ketene intermediates under continuous flow conditions | 2.0 | 12 | Citations (PDF) |
| 13 | Photoredox-Catalyzed Dehydrogenative Csp3–Csp2 Cross-Coupling of Alkylarenes to Aldehydes in Flow | 3.5 | 17 | Citations (PDF) |
| 14 | Enzymatic pretreatment of recycled grease trap waste in batch and continuous-flow reactors for biodiesel production | 12.0 | 17 | Citations (PDF) |
| 15 | A Practical Method for Continuous Production of sp3‐Rich Compounds from (Hetero)Aryl Halides and Redox‐Active Esters | 3.4 | 44 | Citations (PDF) |
| 16 | A tutored discourse on microcontrollers, single board computers and their applications to monitor and control chemical reactions | 2.8 | 18 | Citations (PDF) |
| 17 | Integrated Batch and Continuous Flow Process for the Synthesis of Goniothalamin | 4.2 | 22 | Citations (PDF) |
| 18 | Photoredox Generation of Sulfonyl Radicals and Coupling with Electron Deficient Olefins | 4.8 | 44 | Citations (PDF) |
| 19 | In silico rationalisation of selectivity and reactivity in Pd-catalysed C–H activation reactions | 1.9 | 5 | Citations (PDF) |
| 20 | Living with our machines: Towards a more sustainable future | 5.4 | 10 | Citations (PDF) |
| 21 | Direct Oxidation of Csp3−H bonds using in Situ Generated Trifluoromethylated Dioxirane in Flow | 3.4 | 21 | Citations (PDF) |
| 22 | A Photoredox Coupling Reaction of Benzylboronic Esters and Carbonyl Compounds in Batch and Flow | 4.8 | 30 | Citations (PDF) |
| 23 | Fast continuous alcohol amination employing a hydrogen borrowing protocol | 9.1 | 38 | Citations (PDF) |
| 24 | Enabling synthesis in fragment-based drug discovery by reactivity mapping: photoredox-mediated cross-dehydrogenative heteroarylation of cyclic amines | 7.1 | 102 | Citations (PDF) |
| 25 | Rapid, selective and stable HaloTag-LbADH immobilization directly from crude cell extract for the continuous biocatalytic production of chiral alcohols and epoxides | 2.8 | 38 | Citations (PDF) |
| 26 | Diastereoselective Synthesis of Functionalized Indolines Using in situ Generated Allyl Boronic Species | 1.4 | 10 | Citations (PDF) |
| 27 | Engineering chemistry for the future of chemical synthesis | 2.0 | 69 | Citations (PDF) |
| 28 | Real-Time Spectroscopic Analysis Enabling Quantitative and Safe Consumption of Fluoroform during Nucleophilic Trifluoromethylation in Flow | 6.9 | 60 | Citations (PDF) |
| 29 | Integrated plug flow synthesis and crystallisation of pyrazinamide | 2.8 | 23 | Citations (PDF) |
| 30 | Across‐the‐World Automated Optimization and Continuous‐Flow Synthesis of Pharmaceutical Agents Operating Through a Cloud‐Based Server | 14.4 | 85 | Citations (PDF) |
| 31 | Three-Component Assembly of Multiply Substituted Homoallylic Alcohols and Amines Using a Flow Chemistry Photoreactor | 4.8 | 25 | Citations (PDF) |
| 32 | Across‐the‐World Automated Optimization and Continuous‐Flow Synthesis of Pharmaceutical Agents Operating Through a Cloud‐Based Server | 1.4 | 14 | Citations (PDF) |
| 33 | In-line separation of multicomponent reaction mixtures using a new semi-continuous supercritical fluid chromatography system | 2.8 | 12 | Citations (PDF) |
| 34 | C–H functionalisation of aldehydes using light generated, non-stabilised diazo compounds in flow | 3.4 | 28 | Citations (PDF) |
| 35 | Preparation of homoallylic amines via a three-component coupling process | 2.6 | 11 | Citations (PDF) |
| 36 | Organic photocatalysis for the radical couplings of boronic acid derivatives in batch and flow | 3.4 | 76 | Citations (PDF) |
| 37 | A Convergent Continuous Multistep Process for the Preparation of C4-Oxime-Substituted Thiazoles | 3.4 | 15 | Citations (PDF) |
| 38 | Highly diastereoselective boron and titanium mediated aldol reactions of a mannitol derived 2,3-butanediacetal ethyl ketone | 2.0 | 3 | Citations (PDF) |
| 39 | Mimicking the surface and prebiotic chemistry of early Earth using flow chemistry | 13.7 | 86 | Citations (PDF) |
| 40 | Rapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow‐Generated Diazo Compounds and Propargylated Amines | 1.4 | 13 | Citations (PDF) |
| 41 | Rapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow‐Generated Diazo Compounds and Propargylated Amines | 14.4 | 86 | Citations (PDF) |
| 42 | Utilization of flow chemistry in catalysis: New avenues for the selective synthesis of Bis(indolyl)methanes | 2.0 | 19 | Citations (PDF) |
| 43 | Flow synthesis of cyclobutanones via [2 + 2] cycloaddition of keteneiminium salts and ethylene gas | 2.8 | 17 | Citations (PDF) |
| 44 | One-Pot Acid-Catalyzed Ring-Opening/Cyclization/Oxidation of Aziridines with N-Tosylhydrazones: Access to 1,2,4-Triazines | 4.8 | 57 | Citations (PDF) |
| 45 | A New Methodology for Incorporating Chiral Linkers into Stapled Peptides | 2.6 | 23 | Citations (PDF) |
| 46 | Unveiling the role of boroxines in metal-free carbon–carbon homologations using diazo compounds and boronic acids | 7.1 | 36 | Citations (PDF) |
| 47 | A Versatile Route to Unstable Diazo Compounds via Oxadiazolines and their Use in Aryl–Alkyl Cross‐Coupling Reactions | 14.4 | 76 | Citations (PDF) |
| 48 | A Versatile Route to Unstable Diazo Compounds via Oxadiazolines and their Use in Aryl–Alkyl Cross‐Coupling Reactions | 1.4 | 20 | Citations (PDF) |
| 49 | Continuous direct anodic flow oxidation of aromatic hydrocarbons to benzyl amides | 2.8 | 34 | Citations (PDF) |
| 50 | A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters | 14.4 | 182 | Citations (PDF) |
| 51 | A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters | 1.4 | 30 | Citations (PDF) |
| 52 | Rapid Continuous Ruthenium-Catalysed Transfer Hydrogenation of Aromatic Nitriles to Primary Amines | 1.4 | 11 | Citations (PDF) |
| 53 | Continuous Preparation and Use of Dibromoformaldoxime as a Reactive Intermediate for the Synthesis of 3-Bromoisoxazolines | 3.4 | 22 | Citations (PDF) |
| 54 | Chemoselective Continuous Ru-Catalyzed Hydrogen-Transfer Oppenauer-Type Oxidation of Secondary Alcohols | 3.4 | 26 | Citations (PDF) |
| 55 | Visible-Light-Mediated Annulation of Electron-Rich Alkenes and Nitrogen-Centered Radicals from N-Sulfonylallylamines: Construction of Chloromethylated Pyrrolidine Derivatives | 3.5 | 27 | Citations (PDF) |
| 56 | Flow Chemistry in Europe | 1.7 | 2 | Citations (PDF) |
| 57 | Synthesis of Natural and Unnatural Cyclooligomeric Depsipeptides Enabled by Flow Chemistry | 3.4 | 46 | Citations (PDF) |
| 58 | Solvent-Free Continuous Operations Using Small Footprint Reactors: A Key Approach for Process Intensification | 6.9 | 18 | Citations (PDF) |
| 59 | Synthesis of trifluoromethylated isoxazoles and their elaboration through inter- and intra-molecular C–H arylation | 2.6 | 46 | Citations (PDF) |
| 60 | An Orthogonal Biocatalytic Approach for the Safe Generation and Use of HCN in a Multistep Continuous Preparation of Chiral O-Acetylcyanohydrins | 1.4 | 40 | Citations (PDF) |
| 61 | Identification and Development of 2,3-Dihydropyrrolo[1,2-a]quinazolin-5(1H)-one Inhibitors Targeting Bromodomains within the Switch/Sucrose Nonfermenting Complex | 5.6 | 67 | Citations (PDF) |
| 62 | Engineering chemistry: integrating batch and flow reactions on a single, automated reactor platform | 2.8 | 57 | Citations (PDF) |
| 63 | Visible Light Activation of Boronic Esters Enables Efficient Photoredox C(sp2)–C(sp3) Cross‐Couplings in Flow | 14.4 | 202 | Citations (PDF) |
| 64 | Combination of Enabling Technologies to Improve and Describe the Stereoselectivity of Wolff–Staudinger Cascade Reaction | 2.3 | 49 | Citations (PDF) |
| 65 | A multicomponent approach for the preparation of homoallylic alcohols | 7.1 | 24 | Citations (PDF) |
| 66 | On the Synthesis and Reactivity of 2,3-Dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones | 2.3 | 16 | Citations (PDF) |
| 67 | Continuous Processing and Efficientin SituReaction Monitoring of a Hypervalent Iodine(III) Mediated Cyclopropanation Using Benchtop NMR Spectroscopy | 3.4 | 46 | Citations (PDF) |
| 68 | The Total Synthesis of the Bioactive Natural Product Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B | 3.4 | 11 | Citations (PDF) |
| 69 | Taming hazardous chemistry by continuous flow technology | 37.7 | 673 | Citations (PDF) |
| 70 | Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemia | 10.9 | 105 | Citations (PDF) |
| 71 | Visible Light Activation of Boronic Esters Enables Efficient Photoredox C(sp2)–C(sp3) Cross‐Couplings in Flow | 1.4 | 39 | Citations (PDF) |
| 72 | A Novel Internet-Based Reaction Monitoring, Control and Autonomous Self-Optimization Platform for Chemical Synthesis | 3.4 | 195 | Citations (PDF) |
| 73 | Controlled generation and use of CO in flow | 2.8 | 29 | Citations (PDF) |
| 74 | Iterative reactions of transient boronic acids enable sequential C–C bond formation | 18.7 | 129 | Citations (PDF) |
| 75 | Enabling Technologies for the Future of Chemical Synthesis | 9.2 | 158 | Citations (PDF) |
| 76 | A multistep continuous flow synthesis machine for the preparation of pyrazolesviaa metal-free amine-redox process | 2.8 | 52 | Citations (PDF) |
| 77 | A Versatile Room‐Temperature Route to Di‐ and Trisubstituted Allenes Using Flow‐Generated Diazo Compounds | 14.4 | 101 | Citations (PDF) |
| 78 | Callipeltosides A, B and C: Total Syntheses and Structural Confirmation | 3.4 | 38 | Citations (PDF) |
| 79 | A Versatile Room‐Temperature Route to Di‐ and Trisubstituted Allenes Using Flow‐Generated Diazo Compounds | 1.4 | 23 | Citations (PDF) |
| 80 | Maschinengestützte organische Synthese | 1.4 | 40 | Citations (PDF) |
| 81 | Machine‐Assisted Organic Synthesis | 14.4 | 206 | Citations (PDF) |
| 82 | Development of a flow method for the hydroboration/oxidation of olefins | 2.6 | 20 | Citations (PDF) |
| 83 | A practical deca-gram scale ring expansion of (R)-(−)-carvone to (R)-(+)-3-methyl-6-isopropenyl-cyclohept-3-enone-1 | 2.6 | 19 | Citations (PDF) |
| 84 | Continuous Flow Metathesis for Direct Valorization of Food Waste: An Example of Cocoa Butter Triglyceride | 6.9 | 35 | Citations (PDF) |
| 85 | Total Syntheses of Linear Polythiazole/Oxazole Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B | 1.4 | 6 | Citations (PDF) |
| 86 | Flow Chemistry: Intelligent Processing of Gas–Liquid Transformations Using a Tube-in-Tube Reactor | 17.0 | 284 | Citations (PDF) |
| 87 | Cyclopropanation using flow-generated diazo compounds | 2.6 | 77 | Citations (PDF) |
| 88 | Organic Synthesis: March of the Machines | 14.4 | 437 | Citations (PDF) |
| 89 | Design, Synthesis, and Evaluation of Tetrasubstituted Pyridines as Potent 5-HT2C Receptor Agonists | 3.3 | 13 | Citations (PDF) |
| 90 | Organische Synthese: Vormarsch der Maschinen | 1.4 | 80 | Citations (PDF) |
| 91 | Design, synthesis and evaluation of semi-synthetic triazole-containing caffeic acid analogues as 5-lipoxygenase inhibitors | 5.3 | 32 | Citations (PDF) |
| 92 | Machines vs Malaria: A Flow-Based Preparation of the Drug Candidate OZ439 | 4.8 | 54 | Citations (PDF) |
| 93 | Development of a web-based platform for studying lithiation reactions in silico | 3.4 | 7 | Citations (PDF) |
| 94 | A Systems Approach towards an Intelligent and Self‐Controlling Platform for Integrated Continuous Reaction Sequences | 1.4 | 33 | Citations (PDF) |
| 95 | Generation of Reactive Ketenes under Flow Conditions through Zinc-Mediated Dehalogenation | 1.4 | 34 | Citations (PDF) |
| 96 | Synthesis of a Precursor to Sacubitril Using Enabling Technologies | 4.8 | 41 | Citations (PDF) |
| 97 | Dynamic flow synthesis of porous organic cages | 3.4 | 63 | Citations (PDF) |
| 98 | Modeling mesoscale reactors for the production of fine chemicals | 12.0 | 7 | Citations (PDF) |
| 99 | Flow chemistry as a discovery tool to access sp2–sp3cross-coupling reactions via diazo compounds | 7.1 | 119 | Citations (PDF) |
| 100 | Back Pressure Regulation of Slurry‐Forming Reactions in Continuous Flow | 1.5 | 32 | Citations (PDF) |
| 101 | Total Syntheses of Linear Polythiazole/Oxazole Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B | 14.4 | 34 | Citations (PDF) |
| 102 | A Systems Approach towards an Intelligent and Self‐Controlling Platform for Integrated Continuous Reaction Sequences | 14.4 | 141 | Citations (PDF) |
| 103 | The rapid synthesis of oxazolines and their heterogeneous oxidation to oxazoles under flow conditions | 2.6 | 48 | Citations (PDF) |
| 104 | The Internet of Chemical Things | 0.0 | 12 | Citations (PDF) |
| 105 | Synthesis of Riboflavines, Quinoxalinones and Benzodiazepines through Chemoselective Flow Based Hydrogenations | 4.2 | 29 | Citations (PDF) |
| 106 | Integration of enabling methods for the automated flow preparation of piperazine-2-carboxamide | 1.9 | 69 | Citations (PDF) |
| 107 | Flow‐Based, Cerium Oxide Enhanced, Low‐Level Palladium Sonogashira and Heck Coupling Reactions by Perovskite Catalysts | 2.0 | 19 | Citations (PDF) |
| 108 | Accelerating Spirocyclic Polyketide Synthesis using Flow Chemistry | 14.4 | 125 | Citations (PDF) |
| 109 | Preparation of Unsymmetrical Ketones from Tosylhydrazones and Aromatic Aldehydes via Formyl C–H Bond Insertion | 4.8 | 56 | Citations (PDF) |
| 110 | Metal-Free Coupling of Saturated Heterocyclic Sulfonylhydrazones with Boronic Acids | 3.5 | 96 | Citations (PDF) |
| 111 | Mild and Selective Heterogeneous Catalytic Hydration of Nitriles to Amides by Flowing through Manganese Dioxide | 4.8 | 124 | Citations (PDF) |
| 112 | Highly regioselective lithiation of pyridines bearing an oxetane unit by n-butyllithium | 3.4 | 28 | Citations (PDF) |
| 113 | Continuous flow chemistry: a discovery tool for new chemical reactivity patterns | 2.6 | 72 | Citations (PDF) |
| 114 | Machine-assisted synthesis of modulators of the histone reader BRD9 using flow methods of chemistry and frontal affinity chromatography | 4.5 | 45 | Citations (PDF) |
| 115 | Reconfiguration of a Continuous Flow Platform for Extended Operation: Application to a Cryogenic Fluorine-Directed ortho-Lithiation Reaction | 3.4 | 35 | Citations (PDF) |
| 116 | Design and Application of a Low-Temperature Continuous Flow Chemistry Platform | 3.4 | 55 | Citations (PDF) |
| 117 | Expedient Preparation of Nazlinine and a Small Library of Indole Alkaloids Using Flow Electrochemistry as an Enabling Technology | 4.8 | 92 | Citations (PDF) |
| 118 | Process Intensification for the Continuous Flow Hydrogenation of Ethyl Nicotinate | 3.4 | 72 | Citations (PDF) |
| 119 | A General Continuous Flow Method for Palladium Catalysed Carbonylation Reactions Using Single and Multiple Tube‐in‐Tube Gas‐Liquid Microreactors | 2.3 | 73 | Citations (PDF) |
| 120 | Flow Chemistry Meets Advanced Functional Materials | 3.4 | 122 | Citations (PDF) |
| 121 | Regioselective Preparation of Saturated Spirocyclic and Ring-Expanded Fused Pyrazoles | 3.5 | 39 | Citations (PDF) |
| 122 | Investigation of a Lithium–Halogen Exchange Flow Process for the Preparation of Boronates by Using a Cryo‐Flow Reactor | 3.4 | 41 | Citations (PDF) |
| 123 | Accelerating Spirocyclic Polyketide Synthesis using Flow Chemistry | 1.4 | 28 | Citations (PDF) |
| 124 | Fully Automated Sequence-Specific Synthesis of α-Peptides Using Flow Chemistry | 1.7 | 17 | Citations (PDF) |
| 125 | A prototype device for evaporation in batch and flow chemical processes | 9.1 | 73 | Citations (PDF) |
| 126 | Fragment-based hit identification: thinking in 3D | 6.6 | 155 | Citations (PDF) |
| 127 | Flow chemistry syntheses of natural products | 37.7 | 654 | Citations (PDF) |
| 128 | Continuous Flow-Processing of Organometallic Reagents Using an Advanced Peristaltic Pumping System and the Telescoped Flow Synthesis of (E/Z)-Tamoxifen | 3.4 | 145 | Citations (PDF) |
| 129 | Scaling Up of Continuous Flow Processes with Gases Using a Tube-in-Tube Reactor: Inline Titrations and Fanetizole Synthesis with Ammonia | 3.4 | 77 | Citations (PDF) |
| 130 | An expeditious synthesis of imatinib and analogues utilising flow chemistry methods | 2.6 | 97 | Citations (PDF) |
| 131 | Flow chemistry synthesis of zolpidem, alpidem and other GABAAagonists and their biological evaluation through the use of in-line frontal affinity chromatography | 7.1 | 125 | Citations (PDF) |
| 132 | Flow Chemistry Syntheses of Styrenes, Unsymmetrical Stilbenes and Branched Aldehydes | 3.6 | 70 | Citations (PDF) |
| 133 | Design, Synthesis, and Biological Evaluation of an Allosteric Inhibitor of HSET that Targets Cancer Cells with Supernumerary Centrosomes | 4.7 | 121 | Citations (PDF) |
| 134 | Synthesis of spongistatin 2 employing a new route to the EF fragment | 7.1 | 9 | Citations (PDF) |
| 135 | A Mild and Efficient Flow Procedure for the Transfer Hydrogenation of Ketones and Aldehydes using Hydrous Zirconia | 4.8 | 122 | Citations (PDF) |
| 136 | The synthesis of neurotensin antagonist SR 48692 for prostate cancer research | 2.6 | 16 | Citations (PDF) |
| 137 | A Continuous Flow Solution to Achieving Efficient Aerobic Anti‐Markovnikov Wacker Oxidation | 3.8 | 61 | Citations (PDF) |
| 138 | Flow Synthesis and Biological Studies of an Analgesic Adamantane Derivative That Inhibits P2X7-Evoked Glutamate Release | 3.3 | 18 | Citations (PDF) |
| 139 | Studies of a Diastereoselective Electrophilic Fluorination Reaction Employing a Cryo-Flow Reactor | 1.4 | 10 | Citations (PDF) |
| 140 | Sustainable Flow Oppenauer Oxidation of Secondary Benzylic Alcohols with a Heterogeneous Zirconia Catalyst | 4.8 | 38 | Citations (PDF) |
| 141 | Continuous Cold without Cryogenic Consumables: Development of a Convenient Laboratory Tool for Low‐Temperature Flow Processes | 1.5 | 12 | Citations (PDF) |
| 142 | A Machine‐Assisted Flow Synthesis of SR48692: A Probe for the Investigation of Neurotensin Receptor‐1 | 3.4 | 73 | Citations (PDF) |
| 143 | Synthesis of (-)-Hennoxazole A: Integrating Batch and Flow Chemistry Methods | 1.4 | 25 | Citations (PDF) |
| 144 | The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow | 1.9 | 15 | Citations (PDF) |
| 145 | Camera-enabled techniques for organic synthesis | 1.9 | 79 | Citations (PDF) |
| 146 | Continuous-Flow Processing of Gaseous Ammonia Using a Teflon AF-2400 Tube-in-Tube Reactor: Synthesis of Thioureas and In-Line Titrations | 1.4 | 31 | Citations (PDF) |
| 147 | Scale-Up of Flow-Assisted Synthesis of C2-Symmetric Chiral PyBox Ligands | 2.3 | 9 | Citations (PDF) |
| 148 | Continuous stream processing: a prototype magnetic field induced flow mixer | 2.5 | 9 | Citations (PDF) |
| 149 | Synthesis of Enantiomerically Enriched 3-Amino-2-oxindoles through a Palladium-Mediated Asymmetric Intramolecular Arylation of α-Ketimino Amides | 4.8 | 51 | Citations (PDF) |
| 150 | Continuous Multiple Liquid–Liquid Separation: Diazotization of Amino Acids in Flow | 4.8 | 95 | Citations (PDF) |
| 151 | Synthesis and Use of a Trifluoromethylated Azomethine Ylide Precursor | 3.5 | 38 | Citations (PDF) |
| 152 | Continuous Preparation of Arylmagnesium Reagents in Flow with Inline IR Monitoring | 3.4 | 129 | Citations (PDF) |
| 153 | A-Ring Dihalogenation Increases the Cellular Activity of Combretastatin-Templated Tetrazoles | 3.3 | 45 | Citations (PDF) |
| 154 | Convergent Total Syntheses of Callipeltosides A, B, and C | 14.4 | 33 | Citations (PDF) |
| 155 | A “Catch–React–Release” Method for the Flow Synthesis of 2-Aminopyrimidines and Preparation of the Imatinib Base | 4.8 | 51 | Citations (PDF) |
| 156 | Convergent Total Syntheses of Callipeltosides A, B, and C | 1.4 | 10 | Citations (PDF) |
| 157 | A Total Synthesis of Millingtonine A | 4.8 | 45 | Citations (PDF) |
| 158 | Flow synthesis using gaseous ammonia in a Teflon AF-2400 tube-in-tube reactor: Paal–Knorr pyrrole formation and gas concentration measurement by inline flow titration | 2.6 | 105 | Citations (PDF) |
| 159 | Continuous flow reaction monitoring using an on‐line miniature mass spectrometer | 1.4 | 126 | Citations (PDF) |
| 160 | On Being Green: Can Flow Chemistry Help? | 6.7 | 202 | Citations (PDF) |
| 161 | A prototype continuous-flow liquid–liquid extraction system using open-source technology | 2.6 | 108 | Citations (PDF) |
| 162 | Asymmetric Homogeneous Hydrogenation in Flow using a Tube‐in‐Tube Reactor | 3.8 | 76 | Citations (PDF) |
| 163 | The Oxygen‐Mediated Synthesis of 1,3‐Butadiynes in Continuous Flow: Using Teflon AF‐2400 to Effect Gas/Liquid Contact | 6.2 | 110 | Citations (PDF) |
| 164 | A Flow-Based Synthesis of 2-Aminoadamantane-2-carboxylic Acid | 3.4 | 68 | Citations (PDF) |
| 165 | Increased endothelial cell selectivity of triazole-bridged dihalogenated A-ring analogues of combretastatin A–1 | 2.6 | 24 | Citations (PDF) |
| 166 | A total synthesis of the ammonium ionophore, (−)-enniatin B | 1.4 | 19 | Citations (PDF) |
| 167 | Hydrogenation in flow: Homogeneous and heterogeneous catalysis using Teflon AF-2400 to effect gas–liquid contact at elevated pressure | 7.1 | 205 | Citations (PDF) |
| 168 | The clerodane ring system: investigating the viability of a direct Diels–Alder approach | 2.6 | 12 | Citations (PDF) |
| 169 | Continuous Flow Processing of Slurries: Evaluation of an Agitated Cell Reactor | 3.4 | 152 | Citations (PDF) |
| 170 | Microwave and flow syntheses of Pseudomonasquinolone signal (PQS) and analogues | 2.6 | 52 | Citations (PDF) |
| 171 | Synthesis of a Drug-Like Focused Library of Trisubstituted Pyrrolidines Using Integrated Flow Chemistry and Batch Methods | 4.5 | 44 | Citations (PDF) |
| 172 | The application of a monolithic triphenylphosphine reagent for conducting Appel reactions in flow microreactors | 1.9 | 42 | Citations (PDF) |
| 173 | Safe and Reliable Synthesis of Diazoketones and Quinoxalines in a Continuous Flow Reactor | 4.8 | 138 | Citations (PDF) |
| 174 | Teflon AF-2400 mediated gas–liquid contact in continuous flow methoxycarbonylations and in-line FTIR measurement of CO concentration | 2.6 | 120 | Citations (PDF) |
| 175 | A breakthrough method for the accurate addition of reagents in multi-step segmented flow processing | 7.1 | 116 | Citations (PDF) |
| 176 | A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles | 2.6 | 97 | Citations (PDF) |
| 177 | An overview of the key routes to the best selling 5-membered ring heterocyclic pharmaceuticals | 1.9 | 525 | Citations (PDF) |
| 178 | Piecing together the puzzle: understanding a mild, metal free reduction method for the large scale synthesis of hydrazines | 2.0 | 42 | Citations (PDF) |
| 179 | Piperazic acid-containing natural products: Isolation, biological relevance and total synthesis | 10.6 | 102 | Citations (PDF) |
| 180 | A New Enabling Technology for Convenient Laboratory Scale Continuous Flow Processing at Low Temperatures | 4.8 | 116 | Citations (PDF) |
| 181 | Total syntheses of subereamollines A and B | 2.6 | 36 | Citations (PDF) |
| 182 | Flow synthesis of organic azides and the multistep synthesis of imines and amines using a new monolithic triphenylphosphine reagent | 2.6 | 99 | Citations (PDF) |
| 183 | The Continuous‐Flow Synthesis of Carboxylic Acids using CO2 in a Tube‐In‐Tube Gas Permeable Membrane Reactor | 1.4 | 49 | Citations (PDF) |
| 184 | The Continuous‐Flow Synthesis of Carboxylic Acids using CO2 in a Tube‐In‐Tube Gas Permeable Membrane Reactor | 14.4 | 222 | Citations (PDF) |
| 185 | Total Synthesis of Iso‐ and Bongkrekic Acids: Natural Antibiotics Displaying Potent Antiapoptotic Properties | 3.4 | 32 | Citations (PDF) |
| 186 | Diastereoselective Chain‐Elongation Reactions Using Microreactors for Applications in Complex Molecule Assembly | 3.4 | 44 | Citations (PDF) |
| 187 | Total Synthesis of Chloptosin: A Dimeric Cyclohexapeptide | 3.4 | 43 | Citations (PDF) |
| 188 | An Integrated Flow and Batch-Based Approach for the Synthesis of O-Methyl Siphonazole | 1.4 | 14 | Citations (PDF) |
| 189 | Lesser-Known Enabling Technologies for Organic Synthesis | 2.3 | 25 | Citations (PDF) |
| 190 | Allosteric Modulation of Hormone Release from Thyroxine and Corticosteroid-binding Globulins | 2.2 | 51 | Citations (PDF) |
| 191 | Retinoic acid receptor signaling regulates choroid fissure closure through independent mechanisms in the ventral optic cup and periocular mesenchyme | 7.5 | 109 | Citations (PDF) |
| 192 | The Continuous-Flow Synthesis of Styrenes Using Ethylene in a Palladium-Catalysed Heck Cross-Coupling Reaction | 1.4 | 20 | Citations (PDF) |
| 193 | Oxidation Reactions in Segmented and Continuous Flow Chemical Processing Using an N-(tert-Butyl)phenylsulfinimidoyl Chloride Monolith | 1.4 | 7 | Citations (PDF) |
| 194 | Syngas-Mediated C-C Bond Formation in Flow: Selective Rhodium-Catalysed Hydroformylation of Styrenes | 1.4 | 21 | Citations (PDF) |
| 195 | Synthesis of Highly Substituted Nitropyrrolidines, Nitropyrrolizines and Nitropyrroles via Multicomponent-Multistep Sequences within a Flow Reactor | 0.4 | 19 | Citations (PDF) |
| 196 | A flow-based synthesis of Imatinib: the API of Gleevec | 3.4 | 190 | Citations (PDF) |
| 197 | KMnO4-Mediated Oxidation as a Continuous Flow Process | 4.8 | 216 | Citations (PDF) |
| 198 | The application of flow microreactors to the preparation of a family of casein kinase I inhibitors | 2.6 | 78 | Citations (PDF) |
| 199 | An Asymmetric Tandem Conjugative Addition‐Intramolecular Cyclisation Process to Provide Functionalised 3,6‐Dihydropyrans and 4,5‐Epoxytetrahydropyrans | 2.3 | 26 | Citations (PDF) |
| 200 | A Palladium Wall Coated Microcapillary Reactor for Use in Continuous Flow Transfer Hydrogenation | 3.8 | 44 | Citations (PDF) |
| 201 | Multi‐Step Synthesis by Using Modular Flow Reactors: The Preparation of YneOnes and Their Use in Heterocycle Synthesis | 3.4 | 106 | Citations (PDF) |
| 202 | A Continuous Flow Process Using a Sequence of Microreactors with In‐line IR Analysis for the Preparation of N,N‐Diethyl‐4‐(3‐fluorophenylpiperidin‐4‐ylidenemethyl)benzamide as a Potent and Highly Selective δ‐Opioid Receptor Agonist | 3.4 | 100 | Citations (PDF) |
| 203 | Total Synthesis of Chloptosin | 1.4 | 19 | Citations (PDF) |
| 204 | Total Synthesis of Chloptosin | 14.4 | 66 | Citations (PDF) |
| 205 | Total syntheses of the bromotyrosine-derived natural products ianthelline, 5-bromoverongamine and JBIR-44 | 1.4 | 16 | Citations (PDF) |
| 206 | Trapping of palindromic ligands within native transthyretin prevents amyloid formation | 7.5 | 64 | Citations (PDF) |
| 207 | Synthesis of 3-Nitropyrrolidines via Dipolar Cycloaddition Reactions Using a Modular Flow Reactor | 1.4 | 13 | Citations (PDF) |
| 208 | Enzymatic Oxidative Cyclisation Reactions Leading to Dibenzoazocanes | 1.4 | 4 | Citations (PDF) |
| 209 | A Flow Process Using Microreactors for the Preparation of a Quinolone Derivative as a Potent 5HT1B Antagonist | 1.4 | 10 | Citations (PDF) |
| 210 | Multiple Microcapillary Reactor for Organic Synthesis | 3.8 | 39 | Citations (PDF) |
| 211 | The continuous flow synthesis of butane-2,3-diacetal protected building blocks using microreactors | 2.6 | 50 | Citations (PDF) |
| 212 | ReactIR Flow Cell: A New Analytical Tool for Continuous Flow Chemical Processing | 3.4 | 255 | Citations (PDF) |
| 213 | Preparation of arylsulfonyl chlorides by chlorosulfonylation of in situ generated diazonium salts using a continuous flow reactor | 2.6 | 126 | Citations (PDF) |
| 214 | Flow Ozonolysis Using a Semipermeable Teflon AF-2400 Membrane To Effect Gas−Liquid Contact | 4.8 | 304 | Citations (PDF) |
| 215 | Antivascular and anticancer activity of dihalogenated A-ring analogues of combretastatin A-4 | 4.5 | 25 | Citations (PDF) |
| 216 | Total Synthesis of the Anti-Apoptotic Agents Iso- and Bongkrekic Acids | 4.8 | 94 | Citations (PDF) |
| 217 | The flow synthesis of heterocycles for natural product and medicinal chemistry applications | 2.8 | 157 | Citations (PDF) |
| 218 | A Base-Catalysed One-Pot Three-Component
Coupling Reaction Leading to Nitrosubstituted Pyrroles | 2.3 | 4 | Citations (PDF) |
| 219 | Enantioselective Synthesis of the Lyngbouilloside Macrolactone Core | 1.4 | 2 | Citations (PDF) |
| 220 | Second‐Generation Synthesis of Azadirachtin: A Concise Preparation of the Propargylic Mesylate Fragment | 1.4 | 11 | Citations (PDF) |
| 221 | Total Synthesis of Rapamycin | 3.4 | 65 | Citations (PDF) |
| 222 | AuCl3‐Catalyzed Hydroalkoxylation of Conjugated Alkynoates: Synthesis of Five‐ and Six‐Membered Cyclic Acetals | 2.3 | 45 | Citations (PDF) |
| 223 | Pd‐EnCatTM TPP30 as a Catalyst for the Generation of Highly Functionalized Aryl‐ and Alkenyl‐Substituted Acetylenes via Microwave‐Assisted Sonogashira Type Reactions | 2.3 | 48 | Citations (PDF) |
| 224 | Multistep Synthesis Using Modular Flow Reactors: Bestmann–Ohira Reagent for the Formation of Alkynes and Triazoles | 1.4 | 78 | Citations (PDF) |
| 225 | Second‐Generation Synthesis of Azadirachtin: A Concise Preparation of the Propargylic Mesylate Fragment | 14.4 | 22 | Citations (PDF) |
| 226 | Multistep Synthesis Using Modular Flow Reactors: Bestmann–Ohira Reagent for the Formation of Alkynes and Triazoles | 14.4 | 227 | Citations (PDF) |
| 227 | Development of fluorination methods using continuous-flow microreactors | 2.0 | 152 | Citations (PDF) |
| 228 | A microfluidic flow chemistry platform for organic synthesis: the Hofmann rearrangement | 1.4 | 71 | Citations (PDF) |
| 229 | Total synthesis of the potent antifungal agents bengazole C and E | 0.0 | 7 | Citations (PDF) |
| 230 | Continuous flow based catch and release protocol for the synthesis of α-ketoesters | 1.9 | 38 | Citations (PDF) |
| 231 | Cancer, Chemistry, and the Cell: Molecules that Interact with the Neurotensin Receptors | 3.7 | 71 | Citations (PDF) |
| 232 | Synthesis of acetal protected building blocks using flow chemistry with flow I.R. analysis: preparation of butane-2,3-diacetal tartrates | 2.6 | 72 | Citations (PDF) |
| 233 | Highly diastereoselective desymmetrisation of cyclic meso-anhydrides and derivatisation for use in natural product synthesis | 2.6 | 14 | Citations (PDF) |
| 234 | An efficient and transition metal free protocol for the transfer hydrogenation of ketones as a continuous flow process | 9.1 | 48 | Citations (PDF) |
| 235 | Facile, One‐Step Production of Niacin (Vitamin B3) and Other Nitrogen‐Containing Pharmaceutical Chemicals with a Single‐Site Heterogeneous Catalyst | 3.4 | 31 | Citations (PDF) |
| 236 | A General Organocatalytic Enantioselective Malonate Addition to α,β‐Unsaturated Enones | 3.4 | 92 | Citations (PDF) |
| 237 | The Synthesis of Azadirachtin: A Potent Insect Antifeedant | 3.4 | 62 | Citations (PDF) |
| 238 | Natural‐Product‐Like Spiroketals and Fused Bicyclic Acetals as Potential Therapeutic Agents for B‐Cell Chronic Lymphocytic Leukaemia | 3.1 | 36 | Citations (PDF) |
| 239 | PtCl4‐Catalyzed Domino Synthesis of Fused Bicyclic Acetals | 14.4 | 96 | Citations (PDF) |
| 240 | The Azadirachtin Story | 14.4 | 101 | Citations (PDF) |
| 241 | PtCl4‐Catalyzed Domino Synthesis of Fused Bicyclic Acetals | 1.4 | 31 | Citations (PDF) |
| 242 | Die Azadirachtin‐Story | 1.4 | 7 | Citations (PDF) |
| 243 | Functionalised butanediacetal-protected 1,2-diols as suitable partners for Pd-catalysed cross-coupling reactions | 2.0 | 10 | Citations (PDF) |
| 244 | A new synthesis of (−)-epipyriculol: a phytotoxic metabolite | 2.0 | 14 | Citations (PDF) |
| 245 | Magnesium Nitride as a Convenient Source of Ammonia: Preparation of Primary Amides | 4.8 | 84 | Citations (PDF) |
| 246 | Magnesium Nitride as a Convenient Source of Ammonia: Preparation of Dihydropyridines | 4.8 | 67 | Citations (PDF) |
| 247 | A Bifurcated Pathway to Thiazoles and Imidazoles Using a Modular Flow Microreactor | 4.6 | 49 | Citations (PDF) |
| 248 | A modular flow reactor for performing Curtius rearrangements as a continuous flow process | 2.6 | 129 | Citations (PDF) |
| 249 | Azeotropic reflux chromatography: an efficient solution to a difficult separation in the scale-up synthesis of spongistatin 1 | 2.6 | 7 | Citations (PDF) |
| 250 | Azide monoliths as convenient flow reactors for efficient Curtius rearrangement reactions | 2.6 | 117 | Citations (PDF) |
| 251 | Enantiopure 2-Substituted Glyceraldehyde Derivatives by Aza-Claisen Rearrangement or C-Alkylation of Enamines | 4.8 | 7 | Citations (PDF) |
| 252 | Synthesis of Natural Products from the Indian Neem TreeAzadirachta indica | 4.8 | 27 | Citations (PDF) |
| 253 | FeCl3-Catalysed Cleavage of 1,2-Butanediacetal Protected Diols | 1.4 | 3 | Citations (PDF) |
| 254 | The Use of Diethylaminosulfur Trifluoride (DAST) for Fluorination in a Continuous-Flow Microreactor | 1.4 | 25 | Citations (PDF) |
| 255 | Magnesium Nitride as a Convenient
Source of Ammonia: Preparation of Pyrroles | 1.4 | 14 | Citations (PDF) |
| 256 | A General Organocatalytic Enantioselective Nitrocyclopropanation Reaction | 2.3 | 11 | Citations (PDF) |
| 257 | A New Focused Microwave Approach to the Synthesis of Amino-Substituted Pyrroloisoquinolines and Pyrroloquinolines via a Sequential Multi-Component Coupling Process | 2.3 | 3 | Citations (PDF) |
| 258 | Chromatography-Free Suzuki Reactions Using a Polymer-Assisted Solution-Phase (PASP) Approach | 1.4 | 1 | Citations (PDF) |
| 259 | Chiral Glycolate Equivalents for the Asymmetric Synthesis of α-Hydroxycarbonyl Compounds | 3.7 | 39 | Citations (PDF) |
| 260 | Tagged phosphine reagents to assist reaction work-up by phase-switched scavenging using a modular flow reactor | 2.6 | 59 | Citations (PDF) |
| 261 | Flow and batch mode focused microwave synthesis of 5-amino-4-cyanopyrazoles and their further conversion to 4-aminopyrazolopyrimidines | 2.6 | 82 | Citations (PDF) |
| 262 | A sequential enantioselective, organocatalytic route to chiral 1,2-oxazines and chiral pyridazines | 2.6 | 45 | Citations (PDF) |
| 263 | A Microcapillary Flow Disc Reactor for Organic Synthesis | 3.4 | 135 | Citations (PDF) |
| 264 | Fully Automated Flow-Through Synthesis of Secondary Sulfonamides in a Binary Reactor System | 4.6 | 56 | Citations (PDF) |
| 265 | Continuous Flow Ligand-Free Heck Reactions Using Monolithic Pd [0] Nanoparticles | 3.4 | 137 | Citations (PDF) |
| 266 | [3 + 2] Cycloaddition of acetylenes with azides to give 1,4-disubstituted 1,2,3-triazoles in a modular flow reactor | 2.6 | 130 | Citations (PDF) |
| 267 | Total Synthesis of Thapsigargin, a Potent SERCA Pump Inhibitor | 4.8 | 72 | Citations (PDF) |
| 268 | Design and total synthesis of unnatural analogues of the sub-nanomolar SERCA inhibitor thapsigargin | 2.6 | 22 | Citations (PDF) |
| 269 | Total Synthesis of Potent Antifungal Marine Bisoxazole Natural Products Bengazoles A and B | 3.4 | 58 | Citations (PDF) |
| 270 | Total Synthesis of Five Thapsigargins: Guaianolide Natural Products Exhibiting Sub-Nanomolar SERCA Inhibition | 3.4 | 89 | Citations (PDF) |
| 271 | Identification of a putative azadirachtin-binding complex fromDrosophila Kc167 cells | 1.7 | 26 | Citations (PDF) |
| 272 | Total Synthesis of Rapamycin | 14.4 | 56 | Citations (PDF) |
| 273 | Chemical Variation of Natural-Product-Like Scaffolds: Design, Synthesis, and Biological Activity of Fused Bicyclic Acetal Derivatives | 14.4 | 52 | Citations (PDF) |
| 274 | Synthesis of Azadirachtin: A Long but Successful Journey | 14.4 | 182 | Citations (PDF) |
| 275 | A Relay Route for the Synthesis of Azadirachtin | 14.4 | 77 | Citations (PDF) |
| 276 | Total Synthesis of Rapamycin | 1.4 | 10 | Citations (PDF) |
| 277 | Chemical Variation of Natural-Product-Like Scaffolds: Design, Synthesis, and Biological Activity of Fused Bicyclic Acetal Derivatives | 1.4 | 15 | Citations (PDF) |
| 278 | Synthesis of Azadirachtin: A Long but Successful Journey | 1.4 | 30 | Citations (PDF) |
| 279 | A Relay Route for the Synthesis of Azadirachtin | 1.4 | 26 | Citations (PDF) |
| 280 | Titelbild: Synthesis of Azadirachtin: A Long but Successful Journey (Angew. Chem. 40/2007) | 1.4 | 2 | Citations (PDF) |
| 281 | Optimisation of Conditions forO-Benzyl andN-Benzyloxycarbonyl Protecting Group Removal using an Automated Flow Hydrogenator | 3.8 | 47 | Citations (PDF) |
| 282 | A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly | 3.4 | 320 | Citations (PDF) |
| 283 | Diastereoselective aldol reactions with butane-2,3-diacetal protected glyceraldehyde derivatives | 2.6 | 10 | Citations (PDF) |
| 284 | Chemical variation of natural product-like scaffolds: design and synthesis of spiroketal derivatives | 2.6 | 86 | Citations (PDF) |
| 285 | A new asymmetric organocatalytic nitrocyclopropanation reaction | 3.4 | 85 | Citations (PDF) |
| 286 | A flow reactor process for the synthesis of peptides utilizing immobilized reagents, scavengers and catch and release protocols | 3.4 | 101 | Citations (PDF) |
| 287 | A highly selective, organocatalytic route to chiral 1,2-oxazines from ketones | 3.4 | 61 | Citations (PDF) |
| 288 | A highly enantioselective total synthesis of (+)-goniodiol | 2.6 | 29 | Citations (PDF) |
| 289 | Fully Automated Continuous Flow Synthesis of 4,5-Disubstituted Oxazoles | 4.8 | 125 | Citations (PDF) |
| 290 | Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst | 3.4 | 168 | Citations (PDF) |
| 291 | Double Conjugate Addition of Dithiols to Propargylic Carbonyl Systems To Generate Protected 1,3-Dicarbonyl Compounds | 3.5 | 38 | Citations (PDF) |
| 292 | Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat™ 30NP | 1.9 | 29 | Citations (PDF) |
| 293 | Targeting C-reactive protein for the treatment of cardiovascular disease | 37.9 | 663 | Citations (PDF) |
| 294 | An efficient, asymmetric organocatalyst-mediated conjugate addition of nitroalkanes to unsaturated cyclic and acyclic ketones | 2.6 | 95 | Citations (PDF) |
| 295 | Microwave-Assisted Suzuki Coupling Reactions with an Encapsulated Palladium Catalyst for Batch and Continuous-Flow Transformations | 3.4 | 232 | Citations (PDF) |
| 296 | Stereocontrolled Total Synthesis of Bengazole A: A Marine Bisoxazole Natural Product Displaying Potent Antifungal Properties | 14.4 | 37 | Citations (PDF) |
| 297 | Enantioselective Catalytic Intramolecular Cyclopropanation using Modified Cinchona Alkaloid Organocatalysts | 14.4 | 202 | Citations (PDF) |
| 298 | Stereocontrolled Total Synthesis of Bengazole A: A Marine Bisoxazole Natural Product Displaying Potent Antifungal Properties | 1.4 | 1 | Citations (PDF) |
| 299 | Enantioselective Catalytic Intramolecular Cyclopropanation using Modified Cinchona Alkaloid Organocatalysts | 1.4 | 52 | Citations (PDF) |
| 300 | 8,9,10,10a-Tetrahydro-6H-tetrazolo[1,5-a]pyrrolo[2,1-c]pyrazines: New Heterocyclic Frameworks Generated by an Ugi-Type Multicomponent Reaction | 2.3 | 4 | Citations (PDF) |
| 301 | An Enantioselective Organocatalytic Route to Chiral 3,6-Dihydropyridazines from Aldehydes | 1.4 | 8 | Citations (PDF) |
| 302 | Preparation of the Neolignan Natural Product Grossamide by a Continuous-Flow Process | 1.4 | 21 | Citations (PDF) |
| 303 | Practical Synthesis of (S)-Pyrrolidin-2-yl-1H-tetrazole, Incorporating Efficient Protecting Group Removal by Flow-Reactor Hydrogenolysis | 1.4 | 6 | Citations (PDF) |
| 304 | Stereoselective syntheses of pharmaceutically relevant chiral tetrahydrofurans from (S)- and (R)-glyceraldehyde derivatives | 1.6 | 7 | Citations (PDF) |
| 305 | The rapid preparation of 2-aminosulfonamide-1,3,4-oxadiazoles using polymer-supported reagents and microwave heating | 2.0 | 117 | Citations (PDF) |
| 306 | A phase-switch purification approach for the expedient removal of tagged reagents and scavengers following their application in organic synthesis | 2.6 | 31 | Citations (PDF) |
| 307 | The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin | 14.4 | 54 | Citations (PDF) |
| 308 | Total Synthesis of Antascomicin B | 14.4 | 52 | Citations (PDF) |
| 309 | Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry | 14.4 | 76 | Citations (PDF) |
| 310 | The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin | 1.4 | 11 | Citations (PDF) |
| 311 | Total Synthesis of Antascomicin B | 1.4 | 6 | Citations (PDF) |
| 312 | Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo-Symmetry | 1.4 | 13 | Citations (PDF) |
| 313 | Heterogeneous or Homogeneous? A Case Study Involving Palladium-Containing Perovskites in the Suzuki Reaction | 3.8 | 133 | Citations (PDF) |
| 314 | Stereoselective synthesis of (2S,7S)-7-(4-phenoxymethyl)-2-(1-N-hydroxyureidyl-3-butyn-4-yl)oxepane: a potential anti-asthmatic drug candidate | 1.6 | 6 | Citations (PDF) |
| 315 | Stereoselective synthesis of chiral tetrahydrofurans with potent 5-LO inhibitory activity | 1.6 | 4 | Citations (PDF) |
| 316 | Stereoselective synthesis of (2R,3S,4S,5R)-trans-3,4-dihydroxy-5-(4-fluorophenoxymethyl)-2-(1-N-hydroxyureidyl-3-butyn-4-yl)tetrahydrofuran and (2R,3S,4S,5R)-trans-5-ethynyl-2-(4-fluorophenoxymethyl)-3,4-O-isopropylidene tetrahydrofuran from mannose diacetonide | 1.6 | 7 | Citations (PDF) |
| 317 | Synthesis of the EF Fragment of Spongistatin 1 | 1.4 | 2 | Citations (PDF) |
| 318 | Synthesis of a Ceramide Sphingolipid as a Potential Sex Pheromone of the Hair CrabErimacrus isenbeckiiUsing Butane-2,3-diacetal Desymmetrised Glycolic Acid Building Blocks | 1.4 | 1 | Citations (PDF) |
| 319 | A Homo-Proline Tetrazole as an Improved Organocatalyst for the Asymmetric Michael Addition of Carbonyl Compounds to Nitro-Olefins | 1.4 | 5 | Citations (PDF) |
| 320 | Highly Diastereoselective Desymmetrisation of Cyclicmeso-Anhydrides and Derivatisation to Mono-Protected 1,4-Diols | 1.4 | 0 | Citations (PDF) |
| 321 | Copper- and Palladium-Containing Perovskites: Catalysts for the Ullmann and Sonogashira Reactions | 1.4 | 13 | Citations (PDF) |
| 322 | Development of methods suitable for natural product synthesis: The azadirachtin story | 1.9 | 31 | Citations (PDF) |
| 323 | Michael, Michael–aldol and Michael–Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives | 2.6 | 25 | Citations (PDF) |
| 324 | Formation of 4-Aminopyrimidines via the Trimerization of Nitriles Using Focused Microwave Heating | 4.6 | 28 | Citations (PDF) |
| 325 | Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions | 2.6 | 497 | Citations (PDF) |
| 326 | A Highly Selective, Organocatalytic Route to Chiral Dihydro-1,2-oxazines | 4.8 | 106 | Citations (PDF) |
| 327 | Non-metal-catalysed intramolecular alkyne cyclotrimerization reactions promoted by focussed microwave heating in batch and flow modes | 2.6 | 91 | Citations (PDF) |
| 328 | The use of a continuous flow-reactor employing a mixed hydrogen–liquid flow stream for the efficient reduction of imines to amines | 3.4 | 118 | Citations (PDF) |
| 329 | A versatile organocatalyst for the asymmetric conjugate addition of nitroalkanes to enones | 3.4 | 119 | Citations (PDF) |
| 330 | Synthesis of the Alkaloid Natural Products (+)-Plicane and (−)-Obliquine, Using Polymer-Supported Reagents and Scavengers† | 3.8 | 45 | Citations (PDF) |
| 331 | A Highly Automated, Polymer-Assisted Strategy for the Preparation of 2-Alkylthiobenzimidazoles andN,N‘-Dialkylbenzimidazolin-2-ones | 4.6 | 8 | Citations (PDF) |
| 332 | Total Synthesis of Two Novel Subpicomolar Sarco/Endoplasmatic Reticulum Ca2+-ATPase Inhibitors Designed by an Analysis of the Binding Site of Thapsigargin | 5.6 | 28 | Citations (PDF) |
| 333 | Total synthesis of the Fusarium toxin equisetin | 2.6 | 54 | Citations (PDF) |
| 334 | Efficient batch and continuous flow Suzuki cross-coupling reactions under mild conditions, catalysed by polyurea-encapsulated palladium (ii) acetate and tetra-n-butylammonium salts | 3.4 | 112 | Citations (PDF) |
| 335 | 5-Pyrrolidin-2-yltetrazole: A New, Catalytic, More Soluble Alternative to Proline in an Organocatalytic Asymmetric Mannich-type Reaction | 1.4 | 11 | Citations (PDF) |
| 336 | Preparation of Butane-1,2-diacetal-protected l-Glyceraldehyde from d-Mannitol | 2.3 | 19 | Citations (PDF) |
| 337 | Catalytic Polymer-Supported Potassium Thiophenolate in Methanol as a Method for the Removal of Ester, Amide, and Thioacetate Protecting Groups | 1.4 | 1 | Citations (PDF) |
| 338 | An Intramolecular Organocatalytic Cyclopropanation Reaction | 14.4 | 172 | Citations (PDF) |
| 339 | Enantioselective Organocatalytic Cyclopropanation via Ammonium Ylides | 14.4 | 277 | Citations (PDF) |
| 340 | An Intramolecular Organocatalytic Cyclopropanation Reaction | 1.4 | 46 | Citations (PDF) |
| 341 | Enantioselective Organocatalytic Cyclopropanation via Ammonium Ylides | 1.4 | 72 | Citations (PDF) |
| 342 | Moderne Synthesemethoden: Kupfer-vermittelte C(Aryl)-O-, C(Aryl)-N- und C(Aryl)-S-Verknüpfungen | 1.4 | 5 | Citations (PDF) |
| 343 | Multi-Step Application of Immobilized Reagents and Scavengers: A Total Synthesis of Epothilone C | 3.4 | 87 | Citations (PDF) |
| 344 | Grignard additions to 2-uloses: synthesis of stereochemically pure tertiary alcohols | 1.4 | 22 | Citations (PDF) |
| 345 | The preparation and alkylation of a butanedione-derived chiral glycine equivalent and its use for the synthesis of α-amino acids and α,α-disubstituted amino acids | 2.0 | 20 | Citations (PDF) |
| 346 | Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of furanyl (γ)- and pyranyl (δ)-lactols | 2.6 | 21 | Citations (PDF) |
| 347 | Polymer-assisted, multi-step solution phase synthesis and biological screening of histone deacetylase inhibitors | 2.6 | 17 | Citations (PDF) |
| 348 | 5-Pyrrolidin-2-yltetrazole as an asymmetric organocatalyst for the addition of ketones to nitro-olefins | 3.4 | 209 | Citations (PDF) |
| 349 | Preparation of enantiopure butane-2,3-diacetals of glycolic acid and alkylation reactions leading to α-hydroxyacid and amide derivatives | 2.6 | 46 | Citations (PDF) |
| 350 | Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides | 2.6 | 39 | Citations (PDF) |
| 351 | Synthesis of the thapsigargins | 7.5 | 77 | Citations (PDF) |
| 352 | Fully Automated Polymer-Assisted Synthesis of 1,5-Biaryl Pyrazoles | 4.6 | 29 | Citations (PDF) |
| 353 | Development of an Indole Safety-Catch Linker Using Analytical Constructs | 4.6 | 14 | Citations (PDF) |
| 354 | Microwave assisted Leimgruber–Batcho reaction for the preparation of indoles, azaindoles and pyrroylquinolines | 2.6 | 103 | Citations (PDF) |
| 355 | A concise total synthesis of (+)-okaramine C | 2.6 | 78 | Citations (PDF) |
| 356 | The Synthesis of (-)-Gloeosporone, a Potent Fungal Autoinhibitor of Spore Germination Using a p-Allyltricarbonyl- iron Lactone Complex and a New Reduc- tive Decomplexation Procedure for the Installation of the Embedded 1,7-Diol Component of the Natural Product | 0.4 | 8 | Citations (PDF) |
| 357 | The Use of Butane Diacetals of Glycolic Acid as Precursors for the Synthesis of the Phytotoxic Calmodulin Inhibitor Herbarumin II | 1.8 | 24 | Citations (PDF) |
| 358 | Moderne Synthesemethoden: Kupfer-vermittelte C(Aryl)-O-, C(Aryl)-N- und C(Aryl)-S-Verknüpfungen | 1.4 | 532 | Citations (PDF) |
| 359 | Title is missing! | 1.4 | 16 | Citations (PDF) |
| 360 | A Route to the Thapsigargins from (S)-Carvone Providing a Substrate-Controlled Total Synthesis of Trilobolide, Nortrilobolide, and Thapsivillosin F | 1.4 | 14 | Citations (PDF) |
| 361 | Title is missing! | 1.4 | 27 | Citations (PDF) |
| 362 | Modern Synthetic Methods for Copper-Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation | 14.4 | 2,539 | Citations (PDF) |
| 363 | A Total Synthesis of Epothilones Using Solid-Supported Reagents and Scavengers | 14.4 | 57 | Citations (PDF) |
| 364 | A Route to the Thapsigargins from (S)-Carvone Providing a Substrate-Controlled Total Synthesis of Trilobolide, Nortrilobolide, and Thapsivillosin F | 14.4 | 112 | Citations (PDF) |
| 365 | Organic-Catalyst-Mediated Cyclopropanation Reaction | 14.4 | 181 | Citations (PDF) |
| 366 | A sequential tetra-n-propylammonium perruthenate (TPAP)–Wittig oxidation olefination protocol | 1.4 | 54 | Citations (PDF) |
| 367 | Versatile solid-phase synthesis of secondary amines from alcohols. Development of an N-Boc-(o-nitrobenzene)sulfonamide linker | 1.4 | 13 | Citations (PDF) |
| 368 | Total synthesis of the polyenoyltetramic acid polycephalin C | 2.0 | 20 | Citations (PDF) |
| 369 | Addition of Dithiols to Bis-Ynones: Development of a Versatile Platform for the Synthesis of Polyketide Natural Products | 4.8 | 52 | Citations (PDF) |
| 370 | Synthesis of the C-1−C-28 ABCD Unit of Spongistatin 1 | 4.8 | 91 | Citations (PDF) |
| 371 | Development of β-keto 1,3-dithianes as versatile intermediates for organic synthesis | 2.6 | 75 | Citations (PDF) |
| 372 | A Convenient Route to Enantiomerically Pure 2-Substituted Methyl Glycerate Derivatives | 4.8 | 15 | Citations (PDF) |
| 373 | The synthesis of the anti-malarial natural product polysphorin and analogues using polymer-supported reagents and scavengers | 2.6 | 48 | Citations (PDF) |
| 374 | A Practical and Efficient Synthesis of the C-16−C-28 Spiroketal Fragment (CD) of the Spongistatins | 4.8 | 53 | Citations (PDF) |
| 375 | Recyclable Polyurea-Microencapsulated Pd(0) Nanoparticles: An Efficient Catalyst for Hydrogenolysis of Epoxides | 4.8 | 141 | Citations (PDF) |
| 376 | Synthesis of (−)-Gloeosporone, a fungal autoinhibitor of spore germination using a π-allyltricarbonyliron lactone complex as a templating architecture for 1,7-diol construction | 2.6 | 28 | Citations (PDF) |
| 377 | Palladium-containing perovskites: recoverable and reuseable catalysts for Suzuki couplingsElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b3/b308465e/ | 3.4 | 81 | Citations (PDF) |
| 378 | Use of π-allyltricarbonyliron lactone complexes in the synthesis of taurospongin A: a potent inhibitor of DNA polymerase β and HIV reverse transcriptase | 2.6 | 29 | Citations (PDF) |
| 379 | A rapid stereocontrolled synthesis of the 3a-hydroxy-pyrrolo[2,3-b]indole skeleton, a building block for 10b-hydroxy-pyrazino[1′,2′:1,5]pyrrolo[2,3-b]indole-1,4-diones | 2.6 | 55 | Citations (PDF) |
| 380 | Fully automated multi-step solution phase synthesis using polymer supported reagents: preparation of histone deacetylase inhibitors | 2.6 | 26 | Citations (PDF) |
| 381 | Synthesis of carbohydrate derivatives using solid-phase work-up and scavenging techniques | 2.6 | 15 | Citations (PDF) |
| 382 | Transfer hydrogenation using recyclable polyurea-encapsulated palladium: efficient and chemoselective reduction of aryl ketones | 3.4 | 100 | Citations (PDF) |
| 383 | A 2,3-butanedione protected chiral glycine equivalent—a new building block for the stereoselective synthesis of enantiopure N-protected α-amino acids | 3.4 | 20 | Citations (PDF) |
| 384 | Microencapsulation of Osmium Tetroxide in Polyurea | 4.8 | 106 | Citations (PDF) |
| 385 | Reductive decomplexation of π-allyltricarbonyliron lactone complexes using sodium naphthalenide as a route to stereodefined 1,7-diols and 2,3-diene-1,7-diols | 2.6 | 15 | Citations (PDF) |
| 386 | 1,5-Asymmetric induction of chirality using π-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of α-functionalised carbonyl compounds | 2.6 | 9 | Citations (PDF) |
| 387 | Total Synthesis of the PhytotoxicAgent Herbarumin II Using Butane Diacetals of Glycolic Acid as BuildingBlocks | 1.4 | 2 | Citations (PDF) |
| 388 | Synthesis of Enantiomers ofButane-1,2-diacetal-Protected Glyceraldehyde and of (R,R)-Butane-1,2-diacetal-ProtectedGlycolic Acid | 2.3 | 2 | Citations (PDF) |
| 389 | Enantioselective Synthesis of the Tetrahydrobenzylisoquinoline Alkaloid (-)-Norarmepavine Using Polymer Supported Reagents | 0.4 | 12 | Citations (PDF) |
| 390 | A Polymer-supported Iridium Catalyst for the Stereoselective Isomerisation of Double Bonds | 1.4 | 38 | Citations (PDF) |
| 391 | Highly Diastereoselective Ketone
Aldol Reactions of Butane-2,3-diacetal Desymmetrised Glycolic
Acid | 2.3 | 3 | Citations (PDF) |
| 392 | Application of Polymer-Supported Enzymes and Reagents in the Synthesis of γ-Aminobutyric Acid (GABA) Analogues | 1.4 | 9 | Citations (PDF) |
| 393 | Palladium Acetate in Polyurea Microcapsules: A Recoverable and Reusable Catalyst for Hydrogenations | 1.4 | 10 | Citations (PDF) |
| 394 | Sir Derek Harold Richard Barton. 8 September 1918 – 16 March 1998 | 0.0 | 8 | Citations (PDF) |
| 395 | Synthesis, Structure Revision, and Absolute Configuration of (+)-Didemniserinolipid B, a Serinol Marine Natural Product from a TunicateDidemnumsp. | 4.8 | 67 | Citations (PDF) |
| 396 | Highly Selective Entry to the Azadirachtin Skeleton via a Claisen Rearrangement/Radical Cyclization Sequence | 4.8 | 99 | Citations (PDF) |
| 397 | Synthesis of nornicotine, nicotine and other functionalised derivatives using solid-supported reagents and scavengers | 1.4 | 6 | Citations (PDF) |
| 398 | Total Synthesis of the Cyclic Heptapeptide Argyrin B: A New Potent Inhibitor of T-Cell Independent Antibody Formation | 4.8 | 45 | Citations (PDF) |
| 399 | Encapsulation of palladium in polyurea microcapsules | 3.4 | 182 | Citations (PDF) |
| 400 | A Clean Conversion of Aldehydes to Nitriles Using a Solid-Supported Hydrazine | 1.4 | 33 | Citations (PDF) |
| 401 | The simultaneous use of immobilised reagents for the one-pot conversion of alcohols to carboxylic acids | 1.4 | 34 | Citations (PDF) |
| 402 | Synthesis of taurospongin A: a potent inhibitor of DNA polymerase and HIV reverse transcriptase, using π-allyltricarbonyliron lactone complexes | 3.4 | 14 | Citations (PDF) |
| 403 | Reductive decomplexation of π-allyltricarbonyliron lactone complexes; a new route to stereo-defined 1,7-diols and 2,3-diene-1,7-diols | 3.4 | 6 | Citations (PDF) |
| 404 | Polyurea-encapsulated palladium(ii) acetate: a robust and recyclable catalyst for use in conventional and supercritical mediaElectronic supplementary information (ESI) available: representative experimental procedures. See http://www.rsc.org/suppdata/cc/b2/b200677b/ | 3.4 | 135 | Citations (PDF) |
| 405 | The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol | 1.4 | 13 | Citations (PDF) |
| 406 | Synthesis of the β2Agonist (R)-Salmeterol Using a Sequence of Supported Reagents and Scavenging Agents | 4.8 | 33 | Citations (PDF) |
| 407 | Solid-supported reagents for multi-step organic synthesis: preparation and application | 1.2 | 69 | Citations (PDF) |
| 408 | Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions We gratefully acknowledge financial support from Pfizer Central Research for a Postdoctoral Fellowship (to I.R.B.), the BP endowment and the Novartis Research Fellowship (to S.V.L.), and Pharmacia & Upjohn (to C.P.). | 1.4 | 31 | Citations (PDF) |
| 409 | Total Synthesis of Polycephalin C and Determination of the Absolute Configurations at the 3″,4″ Ring Junction | 1.4 | 9 | Citations (PDF) |
| 410 | Butane-2,3-diacetals of Glyceraldehyde: A Stable Alternative to Glyceraldehyde Acetonide | 1.4 | 10 | Citations (PDF) |
| 411 | The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C | 3.4 | 55 | Citations (PDF) |
| 412 | Analytical Construct Resins for Analysis of Solid-Phase Chemistry | 3.4 | 22 | Citations (PDF) |
| 413 | Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions We gratefully acknowledge financial support from Pfizer Central Research for a Postdoctoral Fellowship (to I.R.B.), the BP endowment and the Novartis Research Fellowship (to S.V.L.), and Pharmacia & Upjohn (to C.P.). | 14.4 | 138 | Citations (PDF) |
| 414 | Total Synthesis of Polycephalin C and Determination of the Absolute Configurations at the 3″,4″ Ring Junction | 14.4 | 35 | Citations (PDF) |
| 415 | Butane-2,3-diacetals of Glyceraldehyde: A Stable Alternative to Glyceraldehyde Acetonide | 14.4 | 52 | Citations (PDF) |
| 416 | Total Synthesis of the Cyclic Peptide Argyrin B | 2.3 | 36 | Citations (PDF) |
| 417 | A polymer-Supported [1,3,2]Oxazaphospholidine for the conversion of isothiocyanates to isocyanides and Their subsequent use in an ugi reaction | 2.0 | 59 | Citations (PDF) |
| 418 | The effects of phytochemical pesticides on the growth of cultured invertebrate and vertebrate cells | 3.5 | 45 | Citations (PDF) |
| 419 | Organic synthesis in a changing world | 6.7 | 34 | Citations (PDF) |
| 420 | Total synthesis of the amaryllidaceae alkaloid (+)-plicamine using solid-supported reagents | 2.0 | 118 | Citations (PDF) |
| 421 | New tools and concepts for modern organic synthesis | 79.7 | 236 | Citations (PDF) |
| 422 | Azadirachtin Disrupts Formation of Organised Microtubule Arrays during Microgametogenesis of Plasmodium berghei | 2.2 | 77 | Citations (PDF) |
| 423 | A concise synthesis of carpanone using solid-supported reagents and scavengers | 1.4 | 94 | Citations (PDF) |
| 424 | A mild, enantioselective synthesis of (R)-salmeterol via sodium borohydride–calcium chloride asymmetric reduction of a phenacyl phenylglycinol derivative | 1.4 | 23 | Citations (PDF) |
| 425 | Highly Diastereoselective Lithium Enolate Aldol Reactions of Butane-2,3-diacetal Desymmetrized Glycolic Acid and Deprotection to Enantiopure anti-2,3-Dihydroxy Esters | 4.8 | 53 | Citations (PDF) |
| 426 | 1,2-Diacetals: A New Opportunity for Organic Synthesis | 52.5 | 169 | Citations (PDF) |
| 427 | Title is missing! | 3.4 | 39 | Citations (PDF) |
| 428 | Development and Application of a Carbonyl-13C-Enriched Backbone Amide Linker for Solid-Phase Reaction Monitoring | 4.6 | 12 | Citations (PDF) |
| 429 | Solid-Phase Development of a 1-Hydroxybenzotriazole Linker for Heterocycle Synthesis Using Analytical Constructs | 4.6 | 19 | Citations (PDF) |
| 430 | Rapid assembly of anti,anti-1,2,3-triol motifs via stereoselective addition of organometallics to aldehydes obtained from (R′,R′,S,R)-2,3-butane diacetal protected butanetetraol derivatives | 1.4 | 9 | Citations (PDF) |
| 431 | The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol | 1.7 | 31 | Citations (PDF) |
| 432 | A polymer-supported thionating reagent | 1.4 | 86 | Citations (PDF) |
| 433 | Highly Diastereoselective Michael Addition Reactions of Butane-2,3-diacetal Desymmetrized Glycolic Acid. Preparation of α-Hydroxy-γ-amino Acid Derivatives | 4.8 | 42 | Citations (PDF) |
| 434 | (–)-(4S)-1-Chloro-3-(2,2-dimethyl-1,3-dioxolan-4-yl)propan-2-one | 0.2 | 0 | Citations (PDF) |
| 435 | Characterization of azadirachtin binding to Sf9 nuclei in vitro | 1.7 | 9 | Citations (PDF) |
| 436 | Immobilisierung durch festphasengebundene Metalle als neuartige Phasenwechselmethode für die organische Synthese | 1.4 | 14 | Citations (PDF) |
| 437 | Butane-2,3-Diacetal-Desymmetrized Glycolic Acid—A New Building Block for the Stereoselective Synthesis of Enantiopureα-Hydroxy Acids | 1.4 | 2 | Citations (PDF) |
| 438 | Consecutive Three- and Four-Component Coupling Reactions with Anions Generated from a Butane Diacetal Desymmetrized Glycolic Acid Derivative | 1.4 | 5 | Citations (PDF) |
| 439 | A New Phase-Switch Method for Application in Organic Synthesis Programs Employing Immobilization through Metal-Chelated Tagging | 14.4 | 46 | Citations (PDF) |
| 440 | Butane-2,3-Diacetal-Desymmetrized Glycolic Acid—A New Building Block for the Stereoselective Synthesis of Enantiopureα-Hydroxy Acids | 14.4 | 53 | Citations (PDF) |
| 441 | Consecutive Three- and Four-Component Coupling Reactions with Anions Generated from a Butane Diacetal Desymmetrized Glycolic Acid Derivative | 14.4 | 32 | Citations (PDF) |
| 442 | Both mosquito-derived xanthurenic acid and a host blood-derived factor regulate gametogenesis of Plasmodium in the midgut of the mosquito | 1.3 | 80 | Citations (PDF) |
| 443 | NEW POLYETHYLENE GLYCOL POLYMERS AS KETAL PROTECTING GROUPS – A POLYMER SUPPORTED APPROACH TO SYMMETRICALLY SUBSTITUTED SPIROKETALS | 1.6 | 16 | Citations (PDF) |
| 444 | Solid-Supported Reagents for the Oxidation of Aldehydes to Carboxylic Acids | 1.4 | 29 | Citations (PDF) |
| 445 | A Concise Synthesis of the Natural Product Carpanone Using Solid-Supported Reagents and Scavengers | 1.4 | 44 | Citations (PDF) |
| 446 | A New Route to Butane-1,2-diacetals and the Development of Alternative Substitution Patterns to Facilitate Differential Protection of the Products | 1.4 | 21 | Citations (PDF) |
| 447 | The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol | 1.7 | 1 | Citations (PDF) |
| 448 | A Short and Efficient Stereoselective Synthesis of the Potent 5-Lipoxygenase Inhibitor CMI-977 | 1.6 | 10 | Citations (PDF) |
| 449 | 1,2-Diacetals in Synthesis: Total Synthesis of a Glycosylphosphatidylinositol Anchor ofTrypanosoma brucei | 3.4 | 100 | Citations (PDF) |
| 450 | Synthesis of High-Mannose Type Neoglycolipids: Active Targeting of Liposomes to Macrophages in Gene Therapy | 3.4 | 46 | Citations (PDF) |
| 451 | Solid-phase reaction monitoring—Chemical derivatization and off-bead analysis | 3.9 | 52 | Citations (PDF) |
| 452 | The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C | 1.4 | 7 | Citations (PDF) |
| 453 | The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C | 14.4 | 33 | Citations (PDF) |
| 454 | Rapid assembly of oligosaccharides: 1,2-diacetal-mediated reactivity tuning in the coupling of glycosyl fluorides | 1.6 | 64 | Citations (PDF) |
| 455 | Polymer-supported reagents for multi-step organic synthesis: application to the synthesis of sildenafil | 2.0 | 103 | Citations (PDF) |
| 456 | Chemo-enzymatic synthesis of fluorinated sugar nucleotide: useful mechanistic Probes for glycosyltransferases | 2.6 | 134 | Citations (PDF) |
| 457 | Chemoenzymatic synthesis of l-galactosylated dimeric Sialyl Lewis X structures employing α-1,3-fucosyltransferase V | 2.6 | 19 | Citations (PDF) |
| 458 | Tri-n-butyl[2-(trimethylsilyl)-ethoxymethoxymethyl]stannane: A Convenient Hydroxymethyl Anion Equivalent | 1.4 | 3 | Citations (PDF) |
| 459 | A Rapid Approach for the Optimisation of Polymer Supported Reagents in Synthesis | 1.4 | 5 | Citations (PDF) |
| 460 | Clean and efficient synthesis of azo dyes using polymer-supported reagents | 9.1 | 43 | Citations (PDF) |
| 461 | A Short Stereoselective Total Synthesis of the Fusarium Toxin Equisetin | 4.8 | 53 | Citations (PDF) |
| 462 | Parallel solution-phase syntheses of functionalised bicyclo[2.2.2]octanes: generation of a library using orchestrated multi-step sequences of polymer-supported reagents and sequesterants | 1.4 | 15 | Citations (PDF) |
| 463 | Reductive decomplexation of π-allyltricarbonyliron lactone complexes: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols | 1.4 | 9 | Citations (PDF) |
| 464 | 1,7-Asymmetric induction of chirality in a Mukaiyama aldol reaction using π-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of α-substituted β-hydroxy carbonyl compounds | 1.4 | 11 | Citations (PDF) |
| 465 | The synthesis of mono- and bicyclic ethers via acid catalysed ring-opening cyclisation of tetrahydropyranyl ether derivatives | 1.4 | 6 | Citations (PDF) |
| 466 | Oxygen to carbon rearrangements of anomerically linked alkenols from tetrahydropyran derivatives: an investigation of the reaction mechanism via a double isotopic labelling crossover study | 1.4 | 16 | Citations (PDF) |
| 467 | Diastereoselective oxygen to carbon rearrangements of anomerically linked enol ethers and the total synthesis of (+)-(S,S )-(cis-6-methyltetrahydropyran-2-yl)acetic acid, a component of civet | 1.4 | 56 | Citations (PDF) |
| 468 | The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol | 1.4 | 8 | Citations (PDF) |
| 469 | A Short and Efficient Stereoselective Synthesis of the Polyhydroxylated Macrolactone (+)-Aspicilin | 4.8 | 61 | Citations (PDF) |
| 470 | Combined Application of Analytical Techniques for the Characterization of Polymer Supported Species | 4.6 | 18 | Citations (PDF) |
| 471 | Multi-step organic synthesis using solid-supported reagents and scavengers: a new paradigm in chemical library generation | 1.4 | 672 | Citations (PDF) |
| 472 | Chemistry of Insect Antifeedants from Azadirachta indica (Part 22): Functionalisation of the Decalin Fragment of Azadirachtin via a Claisen Rearrangement Reaction | 1.4 | 29 | Citations (PDF) |
| 473 | 1,7-Induction of chirality in Mukaiyama aldol reactions using π-allyltricarbonyliron lactone and lactam complexes as chiral templates | 2.0 | 16 | Citations (PDF) |
| 474 | Synthesis of an array of potential matrix metalloproteinase inhibitors using a sequence of polymer-supported reagents | 2.0 | 60 | Citations (PDF) |
| 475 | Synthesis of Glycans from the Glycodelins: Two Undeca-, Two Deca-, Three Nona-, an Octa- and a Heptasaccharide | 3.4 | 42 | Citations (PDF) |
| 476 | Total synthesis of the polyenoyltetramic acid mycotoxin erythroskyrine † | 1.0 | 43 | Citations (PDF) |
| 477 | Synthesis of the alkaloids (±)-oxomaritidine and (±)-epimaritidine using an orchestrated multi-step sequence of polymer supported reagents | 1.0 | 99 | Citations (PDF) |
| 478 | Clean synthesis of α-bromo ketones and their utilisation in the synthesis of 2-alkoxy-2,3-dihydro-2-aryl-1,4-benzodioxanes, 2-amino-4-aryl-1,3-thiazoles and piperidino-2-amino-1,3-thiazoles using polymer-supported reagents | 1.0 | 35 | Citations (PDF) |
| 479 | Dispiroketals in synthesis. Part 24.1 Preparation and use of chiral 2,2′-bis(triisopropylsilyloxymethyl)bi(dihydropyran)s as new protecting and resolving agents for 1,2-diols | 1.0 | 28 | Citations (PDF) |
| 480 | A general and efficient procedure for the preparation of enantiopure anti-1,2-diols—synthesis and utility of (R ′,R ′,S,R)-2,3-butane diacetal protected butane tetrol | 1.0 | 23 | Citations (PDF) |
| 481 | Highly cis- or trans-selective oxygen to carbon rearrangements of anomerically linked 6-substituted tetrahydropyranyl enol ethers | 1.0 | 15 | Citations (PDF) |
| 482 | Preparation of desymmetrised meso-tartrate derivatives—synthesis and utility of (R′,R′,R,S)-2,3-butane diacetal protected dimethyl tartrate | 1.0 | 39 | Citations (PDF) |
| 483 | Use of the Potassium Ion as a Template for the Selective Derivatization of the Antibiotic X-206 | 3.5 | 13 | Citations (PDF) |
| 484 | Chemical synthesis of the N-glycans of gp63, the major surface glycoprotein from Leishmania mexicana amazonensis | 1.0 | 19 | Citations (PDF) |
| 485 | Modified mesoporous silicate MCM-41 materials: immobilised perruthenate—a new highly active heterogeneous oxidation catalyst for clean organic synthesis using molecular oxygen | 3.4 | 101 | Citations (PDF) |
| 486 | Total synthesis of the cholesterol biosynthesis inhibitor 1233A via a (π-allyl)tricarbonyliron lactone complex | 1.0 | 19 | Citations (PDF) |
| 487 | Dispiroketals in synthesis. Part 25.1 Further reactions of dispiroketal protected glycolate to afford optically active 1,2,3,4-tetraols | 1.0 | 18 | Citations (PDF) |
| 488 | New building blocks for efficient and highly diastereoselective polyol production—synthesis and utility of (R ′,R ′,S,S ) and (S′,S′,R,R)-2,3-butane diacetal protected butane tetrol derivatives | 1.0 | 33 | Citations (PDF) |
| 489 | Synthesis of the potent analgesic compound (±)-epibatidine using an orchestrated multi-step sequence of polymer supported reagents | 1.0 | 89 | Citations (PDF) |
| 490 | Three-step synthesis of an array of substituted benzofurans using polymer-supported reagents | 1.0 | 92 | Citations (PDF) |
| 491 | Clean five-step synthesis of an array of 1,2,3,4-tetra-substituted pyrroles using polymer-supported reagents | 1.0 | 68 | Citations (PDF) |
| 492 | Total synthesis of the plasmoidal pigment physarorubinic acid, a polyenoyl tetramic acid | 1.0 | 11 | Citations (PDF) |
| 493 | Polymer-supported hypervalent iodine reagents in ‘clean’ organic synthesis with potential application in combinatorial chemistry | 1.0 | 104 | Citations (PDF) |
| 494 | Effiziente Synthese von Oligosacchariden: Totalsynthese eines Glycosylphosphatidyl- inosit-Ankers ausTrypanosoma brucei | 1.4 | 18 | Citations (PDF) |
| 495 | Rapid Assembly of Oligosaccharides: Total Synthesis of a Glycosylphosphatidylinositol Anchor ofTrypanosoma brucei | 14.4 | 100 | Citations (PDF) |
| 496 | Actions of azadirachtin, a plant allelochemical, against insects | 1.0 | 130 | Citations (PDF) |
| 497 | Stereoelectronic effects in the reactions of conformationally restricted, substituted cyclohexane-1,2-diones with 1,2-diols | 1.6 | 4 | Citations (PDF) |
| 498 | Assembly of dendritic glycoclusters from monomeric mannose building blocks | 1.0 | 28 | Citations (PDF) |
| 499 | Tuning glycoside reactivity: New tool for efficient oligosaccharide synthesis | 1.0 | 271 | Citations (PDF) |
| 500 | Mukaiyama aldol reactions of π-allyltricarbonyliron lactone and lactam complexes bearing trimethylsilyl enol ether side-chains. Not just formal, but genuine 1,7 induction of chirality | 3.4 | 11 | Citations (PDF) |
| 501 | Synthesis of isoxazolidines using polymer supported perruthenate (PSP) | 1.0 | 27 | Citations (PDF) |
| 502 | Double diastereodifferentiation in the Mukaiyama aldol reactions of π-allyltricarbonyliron lactone complexes: 1,7- vs. 1,2-asymmetric induction | 1.0 | 12 | Citations (PDF) |
| 503 | A novel decomplexation of π-allyltricarbonyliron lactone complexes using borohydride reagents: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols | 3.4 | 6 | Citations (PDF) |
| 504 | A new route to functionalised π-allyltricarbonyliron lactam complexes from aziridines and their use in stereoselective synthesis and oxidative conversion to β-lactams | 3.4 | 35 | Citations (PDF) |
| 505 | Clean six-step synthesis of a piperidino-thiomorpholine library using polymer-supported reagents | 1.0 | 44 | Citations (PDF) |
| 506 | Tricarbonyliron complexes: an approach to acyclic stereocontrol | 37.7 | 56 | Citations (PDF) |
| 507 | Synthesis of the acyltetronic acid ionophore tetronasin (ICI M139603) | 1.0 | 33 | Citations (PDF) |
| 508 | A total synthesis of (+)-Goniodiol using an anomeric oxygen-to-carbon rearrangement | 1.0 | 27 | Citations (PDF) |
| 509 | Highly diastereoselective synthesis of β-hydroxy carbonyl compounds using π-allyltricarbonyliron lactone complexes: a formal 1,7-asymmetric induction of chirality in a Mukaiyama aldol reaction | 3.4 | 9 | Citations (PDF) |
| 510 | Development of a polymer bound Wittig reaction and use in multi-step organic synthesis for the overall conversion of alcohols to β-hydroxyamines | 1.0 | 63 | Citations (PDF) |
| 511 | Use of polymer supported reagents for clean multi-step organic synthesis: preparation of amines and amine derivatives from alcohols for use in compound library generation | 1.0 | 45 | Citations (PDF) |
| 512 | Total synthesis of the protein phosphatase inhibitor okadaic acid | 1.0 | 63 | Citations (PDF) |
| 513 | Clean three-step synthesis of 4,5-dihydro-1H-pyrazoles starting from alcohols using polymer supported reagents | 1.0 | 33 | Citations (PDF) |
| 514 | Polymer Supported Perruthenate (PSP): Clean Oxidation of Primary Alcohols to Carbonyl Compounds Using Oxygen as Cooxidant | 2.3 | 98 | Citations (PDF) |
| 515 | Anomeric Oxygen to Carbon Rearrangements of Alkynyl Tributylstannane Derivatives of Lactols | 1.4 | 15 | Citations (PDF) |
| 516 | Studies Towards the Synthesis of the C29-C51 Fragment of Altohyrtin A | 1.4 | 48 | Citations (PDF) |
| 517 | Diastereoselective Anomeric Oxygen to Carbon Rearrangements of Silyl Enol Ether Derivatives of Lactols | 1.4 | 20 | Citations (PDF) |
| 518 | One-pot Synthesis of Penta- and Hepta-saccharides from Monomeric Mannose Building Blocks Using the Principles of Orthogonality and Reactivity Tuning | 1.4 | 42 | Citations (PDF) |
| 519 | A General C-Glycosidation Procedure via Anomeric Oxygen to Carbon Rearrangements of Tetrahydropyranyl Ether Derivatives | 1.4 | 9 | Citations (PDF) |
| 520 | One-Pot Synthesis of Tetra- and Pentasaccharides from Monomeric Building Blocks Using the Principles of Orthogonality and Reactivity Tuning | 1.4 | 44 | Citations (PDF) |
| 521 | 1,5-Asymmetric induction of chirality: highly diastereoselective addition reactions of organoaluminium reagents into ketone groups in the side-chain of π-allyltricarbonyliron lactone complexes | 1.0 | 30 | Citations (PDF) |
| 522 | 1,5-Asymmetric induction of chirality: diastereoselective addition of organoaluminium reagents and allylstannanes into aldehyde groups in the side-chain of π-allyltricarbonyliron lactone complexes | 1.0 | 15 | Citations (PDF) |
| 523 | 1,5-Asymmetric induction of chirality: highly diastereoselective synthesis of homoallylic tertiary alcohols by the Lewis acid-mediated addition of allylstannanes into ketones in the side-chain of π-allyltricarbonyliron lactone complexes | 1.0 | 20 | Citations (PDF) |
| 524 | Synthesis of β-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex | 1.0 | 14 | Citations (PDF) |
| 525 | Rapid access to rare natural pyranosides using 1,2-diacetal protected intermediates | 1.0 | 23 | Citations (PDF) |
| 526 | Polymer supported perruthenate (PSP): a new oxidant for clean organic synthesis | 1.0 | 105 | Citations (PDF) |
| 527 | Direct preparation of diacetals from 1,2-diketones and their use as 1,2-diol protecting groups | 1.0 | 77 | Citations (PDF) |
| 528 | Preparation, structure, derivatisation and NMR data of cyclohexane-1,2-diacetal protected carbohydrates | 1.0 | 44 | Citations (PDF) |
| 529 | Tetra-n-propylammonium perruthenate (TPAP)-catalysed oxidations of alcohols using molecular oxygen as a co-oxidant | 1.0 | 132 | Citations (PDF) |
| 530 | Identification of Azadirachtin in Tissue-Cultured Cells of Neem (Azadirachta Indica) | 0.5 | 17 | Citations (PDF) |
| 531 | Dispiroketals in synthesis. Part 23.1 A new route to (+)-D-conduritol B from myo-inositol | 1.0 | 18 | Citations (PDF) |
| 532 | Characterization of azadirachtin binding to Sf9 nuclei in vitro | 1.7 | 19 | Citations (PDF) |
| 533 | A New Strategy for Oligosaccharide Assembly Exploiting Cyclohexane‐1,2‐diacetal Methodology: An Efficient Synthesis of a High Mannose Type Nonasaccharide | 3.4 | 90 | Citations (PDF) |
| 534 | (π-Allyl)tricarbonyliron Lactone Complexes in Organic Synthesis: A Useful and Conceptually Unusual Route to Lactones and Lactams | 52.5 | 111 | Citations (PDF) |
| 535 | Synthetic studies towards the clerodane insect antifeedant jodrellin A: preparation of a polycyclic model compound with antifeedant activity | 1.0 | 17 | Citations (PDF) |
| 536 | Autoradiographic localization of [22,23-3H2] dihydroazadirachtin binding sites in desert locust testes and effects of Azadirachtin on sperm motility | 2.3 | 32 | Citations (PDF) |
| 537 | Diastereoselective addition reactions of allylstannanes to carbonyl groups in the side-chain of π-allyltricarbonyliron lactone complexes | 3.4 | 9 | Citations (PDF) |
| 538 | Diastereoselective additions to aldehyde groups in the side-chain of π-allyltricarbonyliron lactone complexes | 3.4 | 10 | Citations (PDF) |
| 539 | Chemistry of insect antifeedants from Azadirachta indica(part 20): synthesis of biologically active, simple analogues of azadirachtin, containing the hydroxytetrahydrofurancarboxylate hemiketal moiety | 1.0 | 6 | Citations (PDF) |
| 540 | Chemistry of insect antifeedants from Azadirachta indica(part 21): synthesis of model compounds of azadirachtin using a decalin framework as a functional group scaffolding | 1.0 | 13 | Citations (PDF) |
| 541 | Synthesis and chemistry of the ionophore antibiotic tetronasin | 2.1 | 11 | Citations (PDF) |
| 542 | Synthese des Nonamannan‐Fragmentes eines stark mannosehaltigen Glycoproteins | 1.4 | 13 | Citations (PDF) |
| 543 | Synthesis of the Nonamannan Residue of a Glycoprotein with High Mannose Content | 4.7 | 57 | Citations (PDF) |
| 544 | Dispiroketals in Synthesis (Part 22)1: Use of Chiral 2,2’-Bis(phenylthiomethyl)dihydropyrans as New Protecting and Resolving Agents for 1,2-Diols | 1.4 | 13 | Citations (PDF) |
| 545 | Direct Protection of 1,2-Diols from α-Diketones | 1.4 | 51 | Citations (PDF) |
| 546 | Dispiroketals in Synthesis (Part 21)1: Use of Chiral 2,2’-Bis(halomethyl)dihydropyrans as New Protecting and Resolving Agents for 1,2-Diols | 1.4 | 14 | Citations (PDF) |
| 547 | Dispiroketals in Synthesis (Part 20)1: Preparation of Chiral 2,2’-Bis(halomethyl) and 2,2’-Bis(phenylthiomethyl)dihydropyrans | 1.4 | 17 | Citations (PDF) |
| 548 | Behavioural and neurophysiological responses of Spodoptera littoralis to azadirachtin and a range of synthetic analogues | 1.3 | 32 | Citations (PDF) |
| 549 | Chemistry of insect antifeedants from Azadirachta Indica (part 18): Demethylation and methylation of the C-8 position of the decalin portion of azadirachtin | 2.0 | 26 | Citations (PDF) |
| 550 | Chemistry of insect antifeedants from Azadirachta Indica (Part 19): 1A potential relay route for the synthesis of azadirachtin | 2.0 | 47 | Citations (PDF) |
| 551 | The synthesis and assay of radiolabelled benzene derivatives | 2.0 | 22 | Citations (PDF) |
| 552 | Dispiroketals in synthesis (part 19)1: Dispiroketals as enantioselective and regioselective protective agents for symmetric cyclic and acyclic polyols. | 1.6 | 36 | Citations (PDF) |
| 553 | Spiroketal glycomimetics: the synthesis of a conformationally restrained Sialyl Lewis X mimic | 2.0 | 30 | Citations (PDF) |
| 554 | Biosynthesis of tetronasin: Part 4, preparation of deuterium labelled C19-C26, C17-C26, C11-C26 and C3-C26 polyketide fragments as putative biosynthetic precursors of the ionophore antibiotic tetronasin (ICI 139603) | 2.0 | 12 | Citations (PDF) |
| 555 | Regiospecific fragmentation of benzene derivatives: synthetic and analytical applications | 2.0 | 5 | Citations (PDF) |
| 556 | Behavioural responses of locusts and Spodoptera littoralis to azadirachtin and azadirachtin analogues containing fluorescent and immunogenic reporter groups | 2.1 | 12 | Citations (PDF) |
| 557 | Dispiroketals in Synthesis (Part 18)1: Regioselective and Enantioselective Protection of Symmetric Polyol Substrates Using an Enantiopure (2S,2’S)-Dimethyl-bis-dihydropyran | 1.4 | 4 | Citations (PDF) |
| 558 | Solid Phase Synthesis of Bicyclo[2.2.2]octane Derivatives via Tandem Michael Addition Reactions and Subsequent Reductive Amination | 1.4 | 74 | Citations (PDF) |
| 559 | Tuning the Reactivity of Glycosides: Efficient One-pot Oligosaccharide Synthesis1 | 1.4 | 74 | Citations (PDF) |
| 560 | Dispiroketals: a new functional group for organic synthesis | 1.6 | 38 | Citations (PDF) |
| 561 | Synthesis of β-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex | 1.9 | 4 | Citations (PDF) |
| 562 | Dispiroketals in synthesis (Part 16): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form and their application as bifunctional, C2‐symmetrical, chiral auxiliaries for highly stereoselective Michael additions | 0.0 | 8 | Citations (PDF) |
| 563 | Dispiroketals in Synthesis (Part 15): Simultaneous Enantioselective and Regioselective Protection of Glycerol by Reaction with C2Symmetric (4S,4′S)-Dimethyl-bis-dihydropyran | 2.3 | 20 | Citations (PDF) |
| 564 | Tetrapropylammonium Perruthenate, Pr4N+RuO4
-, TPAP: A Catalytic Oxidant for Organic Synthesis | 2.3 | 1,227 | Citations (PDF) |
| 565 | Dispiroketals in synthesis (part 9): Resolution of 1,2-diols using a C2-symmetric diphenyltetrahydrobipyran. | 1.6 | 18 | Citations (PDF) |
| 566 | Chemistry of insect antifeedants from Azadirachta indica (Part 17): Synthesis of model compounds of azadirachtin. Unusual effect of remote substituents on the course of the oxidative ring contraction reaction. | 2.0 | 13 | Citations (PDF) |
| 567 | “Connectivist” approach to organic structure determination Lsd-program assisted Nmr analysis of the insect antifeedant Azadirachtin | 2.0 | 26 | Citations (PDF) |
| 568 | Studies towards the total synthesis of rapamycin: A convergent and stereoselective synthesis of the C22C32 carbon framework | 1.4 | 43 | Citations (PDF) |
| 569 | Studies towards the total synthesis of rapamycin: Preparation of the cyclohexyl C33C42 fragment and further coupling to afford the C22C42 carbon unit | 1.4 | 22 | Citations (PDF) |
| 570 | Studies towards the total synthesis of rapamycin: Preparation of the C10C17 carbon unit | 1.4 | 29 | Citations (PDF) |
| 571 | Dispiroketals in synthesis (part 6): Highly stereoselective alkylation of dispiroketal protected lactate and glycolate enolates | 1.4 | 38 | Citations (PDF) |
| 572 | Dispiroketals in synthesis (part 7): Protection of D-glucopyranose substrates | 1.4 | 24 | Citations (PDF) |
| 573 | Dispiroketals in synthesis (part 8): Regioselective protection of D-glucopyranose substrates | 1.4 | 34 | Citations (PDF) |
| 574 | Biosynthesis of tetronasin: Part 1 introduction and investigation of the diketide and triketide intermediates bound to the polyketide synthase | 1.4 | 20 | Citations (PDF) |
| 575 | Biosynthesis of tetronasin: Part 2 identification of the tetraketide intermediate attached to the polyketide synthase | 1.4 | 15 | Citations (PDF) |
| 576 | Biosynthesis of tetronasin: Part 3 preparation of deuterium labelled tri- and tetraketides as putative biosynthetic precursors of tetronasin | 1.4 | 16 | Citations (PDF) |
| 577 | Two new routes to the C19C26 tetrahydrofuran fragment of the acyl tetronic acid ionophore tetronasin (ICI M139603) | 1.4 | 19 | Citations (PDF) |
| 578 | Novel polyene cyclisation routes to the acyl tetronic acid ionophore tetronasin (ICI M139603) | 1.4 | 18 | Citations (PDF) |
| 579 | Model studies towards the insect antifeedant Jodrellin A using an organoselenium mediated cyclization reaction | 1.4 | 17 | Citations (PDF) |
| 580 | Towards the synthesis of the C37-C42 fragment of rapamycin: intramolecular reactions of allyl silanes with oxonium ions generated from α-alkoxy sulfones. | 2.0 | 17 | Citations (PDF) |
| 581 | Dispiroketals in synthesis (part 10): Further reactions of dispoke protected lactate and glycolate enolates | 2.0 | 43 | Citations (PDF) |
| 582 | Chemistry of insect antifeedants from Azadirachta indica (Part 16): Synthesis of several derivatives of azadirachtin containing fluorescent or immunogenic reporter groups | 2.0 | 10 | Citations (PDF) |
| 583 | Dispiroketals in synthesis (Part 17): Regioselective protection of D-glucopyranoside D-galactopyranoside and D-mannopyranoside substrates. | 1.6 | 21 | Citations (PDF) |
| 584 | Effect of azadirachtin-derived decalin (perhydronaphthalene) and dihydrofuranacetal (furo[2, 3-fo]pyran) fragments on the feeding behaviour ofSpodoptera littoralis | 1.0 | 23 | Citations (PDF) |
| 585 | Cyclohexane-1,2-diacetals(CDA): A New Protecting Group for Vicinal Diols in Carbohydrates | 4.7 | 76 | Citations (PDF) |
| 586 | A Facile One-Pot Synthesis of a Trisaccharide Unit from the Common Polysaccharide Antigen of Group BStreptococci Using Cyclohexane-1, 2-diacetal(CDA) Protected Rhamnosides | 4.7 | 144 | Citations (PDF) |
| 587 | Cyclohexan‐1,2‐diacetale (CDA): eine neue Schutzgruppe für vicinale Diole in Kohlenhydraten | 1.4 | 30 | Citations (PDF) |
| 588 | Eintopfsynthese einer Trisaccharideinheit des gemeinen Polysaccharid‐Antigens von Streptococci der Gruppe B unter Verwendung Cyclohexan‐1,2‐diacetal(CDA)‐geschützter Rhamnoside | 1.4 | 44 | Citations (PDF) |
| 589 | Dispiroketals in synthesis (Part 11): Concomitant enantioselective and regioselective protection of 2,5- dibenzoyl-myo-inositol | 1.4 | 26 | Citations (PDF) |
| 590 | Dispiroketals in synthesis (Part 12): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form | 1.4 | 23 | Citations (PDF) |
| 591 | Dispiroketals in synthesis (Part 13): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective diels-alder reactions using a bifunctional, C2- symmetrical chiral auxiliary | 1.4 | 20 | Citations (PDF) |
| 592 | Dispiroketals in synthesis (Part 14): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective Michael additions to a bifunctional, C2- symmetrical chiral auxiliary | 1.4 | 23 | Citations (PDF) |
| 593 | Sexual development of malaria parasites is inhibited in vitro by the Neem extract Azadirachtin, and its semi-synthetic analogues | 1.9 | 77 | Citations (PDF) |
| 594 | Diastereoselective addition reactions to carbonyl groups in the side-chain of π-allytricarbonyliron lactone complexes | 1.9 | 24 | Citations (PDF) |
| 595 | Synthesis and chemistry of the insect antifeedant azadirachtin | 1.9 | 29 | Citations (PDF) |
| 596 | Tricarbonyliron lactone complexes in organic synthesis | 1.9 | 23 | Citations (PDF) |
| 597 | Total synthesis of the spiroketal macrolide (+) milbemycin α1 | 1.4 | 12 | Citations (PDF) |
| 598 | Dispiroketals in synthesis (Part 5): A new opportunity for oligosaccharide synthesis using differentially activated glycosyl donors and acceptors | 1.4 | 115 | Citations (PDF) |
| 599 | Dispiroketals in synthesis (part 4): Enantioselective desymmetrization of glycerol using a c2-symmetric disubstituted bis-dihydropyran. | 1.4 | 19 | Citations (PDF) |
| 600 | Chemistry of insect antifeedants from Azadirachta Indica (Part 15):1 Degradation studies of Azadirachtin leading to C8C14 bond cleavage. | 2.0 | 26 | Citations (PDF) |
| 601 | Uptake, retention, metabolism and excretion of [22,23-3H2]dihydroazadirachtin in Schistocerca gregaria | 2.1 | 19 | Citations (PDF) |
| 602 | The chemistry of azadirachtin | 10.6 | 194 | Citations (PDF) |
| 603 | Some Alkylation and Reductive Amination Studies of b-Ketomacrolides as Potential Metal Speciation Materials | 0.4 | 1 | Citations (PDF) |
| 604 | Selective Acylation and Alkylation Reactions of Diols Using Dibutyltin Dimethoxide | 1.4 | 52 | Citations (PDF) |
| 605 | Microwave Promoted Hydrolysis of Esters Absorbed on Alumina: A New Deprotection Method for Pivaloyl Groups | 1.4 | 32 | Citations (PDF) |
| 606 | Dispiroketals in Synthesis (Part 3):1Selective Protection of Diequatorial Vicinal Diols in Carbohydrates | 2.3 | 26 | Citations (PDF) |
| 607 | Synthesis of 4-Substituted Imidazoles via 4-Metallo Imidazole Intermediates | 1.4 | 19 | Citations (PDF) |
| 608 | Total Synthesis of the Carboxylic Acid lonophore Antibiotic CP-61,405 (Routiennocin): Preparation of the Inherent Spiroketal Unit via a Reverse Coupling Process | 1.4 | 13 | Citations (PDF) |
| 609 | Microbial Oxidation in Synthesis: Preparation of Pseudo-α-D-glucopyranose from Benzene | 1.4 | 26 | Citations (PDF) |
| 610 | Microbial Oxidation in Synthesis: Preparation of a Potential Insulin Mimic from Benzene | 1.4 | 22 | Citations (PDF) |
| 611 | Dispiroketals in Synthesis: Preparation of a Stable, Sterically Demanding Glyceraldehyde Ketal and Diastereoselective Reactions with Simple Organometallic Reagents | 2.3 | 49 | Citations (PDF) |
| 612 | Total Synthesis of the Carboxylic Acid Ionophore Antibiotic CP-61,405 (Routiennocin) | 1.4 | 45 | Citations (PDF) |
| 613 | Luminescence dynamics and carbon-13 NMR characteristics of dinuclear complexes exhibiting coupled lanthanide(III) cation pairs | 3.1 | 38 | Citations (PDF) |
| 614 | Clerodane diterpenoids | 10.6 | 380 | Citations (PDF) |
| 615 | Oxidation of Activated Halides to Aldehydes and Ketones by N-Methylmorpholine-N-oxide | 1.6 | 49 | Citations (PDF) |
| 616 | Chemistry of insect antifeedants from Azadirachta indica, Part 14: absolute configuration of azadirachtin | 1.9 | 19 | Citations (PDF) |
| 617 | Chemistry of insect antifeedants from Azadirachta indica(part 13): on the use of the intramolecular Diels–Alder reaction for the construction of trans-fused hydrobenzofuran fragments for azadirachtin synthesis | 1.0 | 7 | Citations (PDF) |
| 618 | Chemistry of insect antifeedants from Azadirachta indica(part 12): use of silicon as a control element in the synthesis of a highly functionalized decalin fragment of azadirachtin | 1.0 | 61 | Citations (PDF) |
| 619 | Immobilization of thallium by tandem oxidation/reduction-complexation of thallium(I/III) | 4.6 | 41 | Citations (PDF) |
| 620 | Total synthesis of the ionophore antibiotic CP-61,405 (routiennocin) | 2.0 | 106 | Citations (PDF) |
| 621 | Dispiroketals in synthesis (part 2): A new group for the selective protection of diequatorial vicinal diols in carbohydrates. | 1.4 | 64 | Citations (PDF) |
| 622 | Further reactions of t-butyl 3-oxobutanthioate and t-butyl 4-diethyl-phosphono-3-oxobutanthioate : Carbonyl coupling reactions, amination, use in the preparation of 3-acyltetramic acids and application to the total synthesis of fuligorubin A. | 2.0 | 128 | Citations (PDF) |
| 623 | New Routes to Biologically Active Heterocyclic Natural Products | 0.0 | 1 | Citations (PDF) |
| 624 | Total synthesis of the anthelmintic macrolide avermectin B1a | 1.0 | 111 | Citations (PDF) |
| 625 | Chemistry of insect antifeedants from azadirachta indica (Part 9): oxidative reactions of azadirachtin derivatives leading to C8-C14 bond cleavage. | 1.4 | 23 | Citations (PDF) |
| 626 | Chemistry of insect antifeedants from Azadirachta indica (Part 10): synthesis of a highly functionalised decalin fragment of azadirachtin. | 1.4 | 34 | Citations (PDF) |
| 627 | Synthesis of the alkaloids (−)-heliotridane and (−)-isoretronecanol via π-allyltricarbonyliron lactam complexes. | 1.4 | 39 | Citations (PDF) |
| 628 | Chemistry of insect antifeedants from Azadirachta indica (part 11): Characterisation and structure activity relationships of some novel rearranged azadirachtins. | 2.0 | 26 | Citations (PDF) |
| 629 | The total synthesis of agglomerin A and (±)-carolinic acid. A general method for the preparation of 3-acyl tetronic acids via direct acylation of O-methyl 3-stannyl tetronates | 2.0 | 56 | Citations (PDF) |
| 630 | Synthesis of the β-lactone esterase inhibitor valilactone using π-allyltricarbonyliron lactone complexes. | 1.4 | 34 | Citations (PDF) |
| 631 | The use of π-allyltricarbonyliron lactone complexes in the synthesis of the β-lactone esterase inhibitor (−)-valilactone. | 2.0 | 58 | Citations (PDF) |
| 632 | Chemistry of insect antifeedants from azadirachta indica (part 8): Synthesis of hydroxydihydrofuran acetal fragments for biological evaluation and azadirachtin total synthesis studies. | 2.0 | 37 | Citations (PDF) |
| 633 | Substitution reactions of 2-phenylsulphonyl-piperidines and -pyrrolidines with carbon nucleophiles: Synthesis of the pyrrolidine alkaloids norruspoline and ruspolinone | 2.0 | 85 | Citations (PDF) |
| 634 | Use of 2-phenylsulphonyl cyclic ethers in the preparation of tetrahydropyran and tetrahydrofuran acetals and in some glycosidation reactions. | 2.0 | 58 | Citations (PDF) |
| 635 | Use of Phenylsulphonylmethano Ethers in Synthesis: A New Versatile Route to Substituted Cyclic Ethers | 1.4 | 11 | Citations (PDF) |
| 636 | Microbial Oxidation in Synthesis: Preparation of Novel 3-Substitutedcis-Cyclohexa-3,5-diene-1,2-diol Derivatives from (1S,2S)-3-Bromocyclohexa-3,5-diene-1,2-diol | 1.4 | 0 | Citations (PDF) |
| 637 | Microbial Oxidation in Synthesis: Preparation of Novel 3-Substituted cis-Cyclohexa-3,5-diene-1,2-diol Derivatives from (1S,2S)-3-Bromocyclohexa-3,5-diene-1,2-diol | 1.4 | 0 | Citations (PDF) |
| 638 | Stereoselective synthesis of inositol phosphates | 1.9 | 37 | Citations (PDF) |
| 639 | Chemistry of insect antifeedants from azadirachta indica (part 6): Synthesis of an optically pure acetal intermediate for potential use in the synthesis of azadirachtin and novel antifeedants. | 1.4 | 25 | Citations (PDF) |
| 640 | Antifeedant effects of azadirachtin and structurally related compounds on lepidopterous larvae | 1.3 | 132 | Citations (PDF) |
| 641 | Azadirachtin: structural requirements for reducing growth and increasing mortality in lepidopterous larvae | 1.3 | 57 | Citations (PDF) |
| 642 | Assessment of butene-1,4-diols as starting materials for the preparation of π-Allyltricarbonyliron complexes | 2.0 | 47 | Citations (PDF) |
| 643 | Chemistry of insect antifeedants from azadirachta indica (part 7): Preparation of an optically pure hydroxyacetal epoxide related to azadirachtin. | 1.4 | 18 | Citations (PDF) |
| 644 | Synthesis of a C16–C28 spiroacetal fragment of avermectin B1a and reassignment of some 1H and 13C resonances of avermectin B1a | 1.4 | 25 | Citations (PDF) |
| 645 | Enantioselective synthesis of the C3-C11 hydrocarbon fragment of the ionophore antibiotic tetronasin (ici 139603). | 1.4 | 16 | Citations (PDF) |
| 646 | Synthesis of the C12–C26 fragment of the acyltetronic acid lonophore antibiotic tetronasin (ici 139603) | 1.4 | 21 | Citations (PDF) |
| 647 | Microbial oxidation in synthesis: preparation of myo-inositol phosphates and related cyclitol derivatives from benzene | 2.0 | 90 | Citations (PDF) |
| 648 | Neo-clerodane insect antifeedants from Scutellaria galericulata | 3.0 | 75 | Citations (PDF) |
| 649 | Direct Substitution of 2-Benzenesulphonylpiperidines and -pyrrolidines by Carbon Nucleophiles: Synthesis of the Pyrrolidine Alkaloid Ruspolinone | 1.4 | 25 | Citations (PDF) |
| 650 | Total Synthesis of Avermectin B1a: Planning of the Synthesis and Preparation of the C1-C10 "Southern" Hydrobenzofuran Fragment | 1.4 | 19 | Citations (PDF) |
| 651 | Alkenylcyclic Sulphites as Novel Precursors for the Preparation of π-Allyltricarbonyliron Lactone Complexes | 1.4 | 22 | Citations (PDF) |
| 652 | Total Synthesis of Avermectin B1a: Synthesis of the C11-C25 Spiroacetal Fragment | 1.4 | 28 | Citations (PDF) |
| 653 | Microbial Oxidation in Synthesis: Concise Preparation of (+)-Conduritol F from Benzene | 1.4 | 30 | Citations (PDF) |
| 654 | Total Synthesis of Avermectin B1a: Final Coupling Reactions and the Total Synthesis of Avermectin B1a Aglycone | 1.4 | 20 | Citations (PDF) |
| 655 | Direct Substitution of 2-Phenylsulphonylpyrrolidines, -piperidines, -tetrahydrofurans and -tetrahydropyrans by Alkyl Organometallic Reagents in Dichloromethane | 1.4 | 25 | Citations (PDF) |
| 656 | An Efficient Three-Step Synthesis of L-(-)-Oleandrose from (S)-(-)-Methyl Lactate | 1.4 | 14 | Citations (PDF) |
| 657 | Total Synthesis of Avermectin B1a: Synthesis of the CarbohydrateBis-Oleandrose Fragment and Coupling to the Avermectin B1a Aglycone | 1.4 | 48 | Citations (PDF) |
| 658 | A Simple, One-Pot, Glycosidation Procedurevia(1-Imidazolylcaronyl) Glycosides and Zinc Bromide | 1.4 | 41 | Citations (PDF) |
| 659 | A new ruthenium(VI) oxidant: preparation, X-ray crystal structure, and properties of (Ph4P)[RuO2(OAc)Cl2] | 1.9 | 32 | Citations (PDF) |
| 660 | The antifeedant activity of clerodane diterpenoids from Teucrium | 3.0 | 100 | Citations (PDF) |
| 661 | The structure of two new clerodane diterpenoid potent insect antifeedants from Scutellaria woronowii (Juz); jodrellin A & B | 1.4 | 66 | Citations (PDF) |
| 662 | Chemistry of insect antifeedants from azadirachta indica (part 4): synthesis towards the limonoid azadirachtin; preparation of a functionalised decalin fragment | 2.0 | 35 | Citations (PDF) |
| 663 | Microbial Oxidation in Synthesis: Preparation of (+)- and (−)-Pinitol from Benzene | 2.0 | 88 | Citations (PDF) |
| 664 | Insect antifeedants from azadirachta indica (part 5): Chemical modification and structure-activity relationships of azadirachtin and some related limonoids | 2.0 | 60 | Citations (PDF) |
| 665 | Substitution reactions of 2-benzenesulphonyl cyclic ethers with carbon nucleophiles | 2.0 | 112 | Citations (PDF) |
| 666 | A highly convergent total synthesis of the spiroacetal macrolide (+)-milbemycinβ1 | 2.0 | 94 | Citations (PDF) |
| 667 | Preparation of β-ketomacrolactones and β-ketodiolides using S-t-butyl 3-oxobutanethioate and S-t-butyl 4-diethylphosphono-3-oxobutanethioate | 2.0 | 19 | Citations (PDF) |
| 668 | Preparation of O-methyl 3-acyl tetronic acids by the direct acylation of stannyl tetronates | 1.4 | 31 | Citations (PDF) |
| 669 | Total synthesis of (+)-milbemycin β1 | 1.4 | 20 | Citations (PDF) |
| 670 | Microbial oxidation in synthesis: Preparation of 6-deoxy cyclitol analogues of myo-inositol 1,4,5-trisphosphate from benzene | 1.4 | 43 | Citations (PDF) |
| 671 | The first crystal and molecular structure of lanthanide homodinuclear macrocyclic complexes showing metal–metal pair interactions | 1.9 | 45 | Citations (PDF) |
| 672 | Recent developments in natural product synthesis | 1.9 | 11 | Citations (PDF) |
| 673 | Substitution Reactions of 2-Benzensulphonyl Cyclic Ethers with Silyl Enol Ethers Promoted by Aluminium Trichloride | 0.4 | 15 | Citations (PDF) |
| 674 | Insect antifeedants: a behavioural and electrophysiological investigation of natural and synthetically derived clerodane diterpenoids | 1.3 | 74 | Citations (PDF) |
| 675 | Activity of drimane antifeedants and related compounds against aphids, and comparative biological effects and chemical reactivity of (?)- and (+)-polygodial | 1.4 | 101 | Citations (PDF) |
| 676 | Preparation of cyclic ether acetals from 2-benzenesulphonylderivatives: a new mild glycosidation procedure | 1.4 | 53 | Citations (PDF) |
| 677 | Microbial oxidation in synthesis: Preparation from benzene of the cellular secondary messenger myo-inositol-1,4,5-trisphosphate (IP3) and related derivatives | 1.4 | 58 | Citations (PDF) |
| 678 | Chemistry of insect antifeedants from (part 1): Conversion from the azadirachtin to the azadirachtinin skeletons | 1.4 | 25 | Citations (PDF) |
| 679 | Chemistry of insect antifeedants from (part 2): Synthesis of a polyoxygenated decalin with limonoid structural homology. | 1.4 | 23 | Citations (PDF) |
| 680 | Use of t-butyl 4-diethylphosphono-3-oxobutanethioate for tetramic acid synthesis: Total synthesis of the plasmodial pigment fuligorubin A | 1.4 | 32 | Citations (PDF) |
| 681 | Chemistry of insect antifeedants from azadirachta indica (part 3): reactions on the C-22,23 enol ether double bond of azadirachtin and conversion to 22,23-dihydro-23-β-methoxyazadirachtin. | 1.4 | 32 | Citations (PDF) |
| 682 | Direct substitution of 2-benzenesulphonyl cyclic ethers using organozinc reagents | 1.4 | 59 | Citations (PDF) |
| 683 | Organic synthesis with tricarbonyliron lactone complexes | 1.0 | 27 | Citations (PDF) |
| 684 | An electrophysiological and behavioural study of insect antifeedant properties of natural and synthetic drimane‐related compounds | 1.9 | 82 | Citations (PDF) |
| 685 | Preparation and use of tetra-n-butylammonium per-ruthenate (TBAP reagent) and tetra-n-propylammonium per-ruthenate (TPAP reagent) as new catalytic oxidants for alcohols | 1.9 | 661 | Citations (PDF) |
| 686 | Use of S-t-butyl acetothioacetate in the preparation of milbemycin seco-analogues | 1.0 | 7 | Citations (PDF) |
| 687 | Preparation of acyltetronic acids using t-butyl acetothioacetate: total synthesis of the fungal metabolites carolic, carlosic, and carlic acids | 1.0 | 62 | Citations (PDF) |
| 688 | Title is missing! | 2.0 | 116 | Citations (PDF) |
| 689 | Synthesis of a hydroxy dihydrofuran acetal related to azadirachtin: A potent insect antifeedant | 1.4 | 0 | Citations (PDF) |
| 690 | Synthesis of a hydroxy dihydrofuran acetal related to azadirachtin: A potent insect antifeedant | 1.4 | 92 | Citations (PDF) |
| 691 | Microbial oxidation in synthesis: A six step perparation of (+)-pinitol from benzene | 1.4 | 136 | Citations (PDF) |
| 692 | Preparation of t-butyl 4-diethylphosphono-3-oxobutanethioate and use in the synthesis of (E)-4-alkenyl-3-oxoesters and macrolides | 1.4 | 40 | Citations (PDF) |
| 693 | The use of β-ketothioesters for the exceptionally mild preparation of β-ketoamides | 1.4 | 56 | Citations (PDF) |
| 694 | A conformational study of bafilomycin A1 by x-ray crystallography and nmr techniques | 1.4 | 63 | Citations (PDF) |
| 695 | Synthesis of the monocyclic nonaromatic C-1 to C-10 fragments of the milbemycins and avermectins. | 1.4 | 19 | Citations (PDF) |
| 696 | Synthesis of a novel 3, 4-dihydromilbemycin analogue. | 1.4 | 12 | Citations (PDF) |
| 697 | Development of a synthetic route towards milbemycin β1: Preparation of an advanced model system. | 1.4 | 13 | Citations (PDF) |
| 698 | Progress towards avermectins and milbemycins | 1.0 | 1 | Citations (PDF) |
| 699 | Synthestic approaches to the teleocidin-related tumour promoters: a total synthesis of (±)-indolactam V | 1.9 | 50 | Citations (PDF) |
| 700 | The synthesis of trisubstituted tetrahydrofurans via the use of an organoselenium-mediated cyclisation reaction | 1.0 | 25 | Citations (PDF) |
| 701 | X-Ray crystallographic structure determination of detigloyldihydroazadirachtin and reassignment of the structure of the limonoid insect antifeedant azadirachtin | 1.9 | 70 | Citations (PDF) |
| 702 | Application of ultrasound to the preparation of tricarbonyliron diene complexes | 2.1 | 38 | Citations (PDF) |
| 703 | Ultrasonic formation and reactions of sodium phenylselenide | 2.0 | 50 | Citations (PDF) |
| 704 | Preparation of 2-substituted pyrroles and indoles by regioselective alkylation and deprotection of 1-(2-trimethylsilylethoxymethyl)pyrrole and 1-(2-trimethylsilylethoxymethyl) indole | 2.0 | 60 | Citations (PDF) |
| 705 | Title is missing! | 2.0 | 70 | Citations (PDF) |
| 706 | Synthetic studies towards the acyltetronic acid iohophore M 139603 | 1.4 | 30 | Citations (PDF) |
| 707 | Preparation of spiroketals by reaction of anions from 2-benzenesulphonyltetrahydropyrans with epoxides: synthesis of the c-11 to c-25 fragment of the milbemycins | 1.4 | 67 | Citations (PDF) |
| 708 | Alkylation reactions of anions derived from 2-benzenesulphonyl tetrahydropyran and their application to spiroketal syntiesis | 2.0 | 88 | Citations (PDF) |
| 709 | Preparation of vinylic sulphones by Peterson olefination using phenyl trimethylsilylmethyl sulphone | 1.0 | 27 | Citations (PDF) |
| 710 | Preparation and reactions of 2-benzenesulphonyltetrahydropyran | 1.4 | 63 | Citations (PDF) |
| 711 | Synthesis of the northern hemisphere of the milbemycins using a new strategy for the formation of the C15 to C16 bond. | 1.4 | 25 | Citations (PDF) |
| 712 | Wittig and horner-wittig coupling reactions of 2-substituted cyclic ethers and their application to spiroketal synthesis | 2.0 | 68 | Citations (PDF) |
| 713 | Synthesis of the β-lactam antibiotic (+)- thienamycin via an intermediate π-allyltricarbonyliron lactone complex | 2.0 | 38 | Citations (PDF) |
| 714 | Total synthesis of the sesquiterpene (±)-hirsutene using an organoselenium-mediated cyclization reaction | 2.0 | 36 | Citations (PDF) |
| 715 | Natural product synthesis using π-allyltricarbonyliron lactone complexes: Synthesis of parasorbic acid, the carpenter bee pheromone and malyngolide | 2.1 | 32 | Citations (PDF) |
| 716 | Use of π-allyltricarbonyliron lactam complexes in the preparation of nocardicin derivatives: synthesis of (–)-3-oxo-1-[(p-benzyloxyphenyl)-benzyloxycarbonylmethyl]azetidin-2-one | 1.0 | 20 | Citations (PDF) |
| 717 | The use of t-butyl acetothioacetate as a route to bis-β-ketomacrolides | 1.9 | 11 | Citations (PDF) |
| 718 | Structural reappraisal of the limonoid insect antifeedant azadirachtin | 1.9 | 28 | Citations (PDF) |
| 719 | Synthesis of (±)-cis-6-methyltetrahydropyran-2-ylacetic acid, a natural product from Viverra civetta, using organoselenium-mediated cyclisation reactions | 1.0 | 8 | Citations (PDF) |
| 720 | Oxo complexes of ruthenium(VI) and (VII) as organic oxidants | 1.0 | 99 | Citations (PDF) |
| 721 | Novel rearrangement of the ionophore antibiotic X-14547A (indanomycin) and related derivatives induced by lithium tetrafluoroborate | 1.0 | 2 | Citations (PDF) |
| 722 | Synthesis of spiroacetals using organoselenium-mediated cyclisation reactions. X-Ray molecular structure of (2S,8R)-8-methyl-2-phenyl-1,7-dioxaspiro[5.5]undecan-4(R)-ol | 1.0 | 30 | Citations (PDF) |
| 723 | Synthesis of the spiroacetal unit related to the avermectins and milbemycins | 1.9 | 26 | Citations (PDF) |
| 724 | Fe2(co)g in tetrahydrofuran or under sonochemical conditions as convenient practical routes to π-allyltricarbonyliron lactone complexes | 2.0 | 41 | Citations (PDF) |
| 725 | A new route to spiro-ketals using the Horner-Wittig reaction of 2-diphenylphosphinoxy cyclic ethers | 1.4 | 46 | Citations (PDF) |
| 726 | Total synthesis of the ionophore antibiotic X-14547A (Indanomycin) | 3.5 | 85 | Citations (PDF) |
| 727 | π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin | 1.9 | 25 | Citations (PDF) |
| 728 | The use of 3-acetoxy-1-trimethylsilylbutadiene in the synthesis of anthracyclinone derivatives | 1.0 | 8 | Citations (PDF) |
| 729 | The Diels–Alder route to drimane related sesquiterpenes; synthesis of cinnamolide, polygodial, isodrimeninol, drimenin and warburganal | 1.0 | 108 | Citations (PDF) |
| 730 | Regiospecific alkylation of β-ketothioesters and use in the synthesis of acyl-tetronic acids | 1.4 | 20 | Citations (PDF) |
| 731 | Total synthesis of the structurally unique ionophore antibiotic X–14547 A | 1.9 | 51 | Citations (PDF) |
| 732 | Peterson olefination using phenylsulphonyltrimethylsilylmethane. A new preparation of vinylic sulphones | 1.9 | 37 | Citations (PDF) |
| 733 | The total synthesis of the clerodane diterpene insect antifeedant ajugarin I | 1.9 | 38 | Citations (PDF) |
| 734 | Synthesis of the drimane-related sesquiterpenes euryfuran, confertifolin, and valdiviolide | 1.0 | 19 | Citations (PDF) |
| 735 | Synthesis of β-lactams from π-allyltricarbonyliron (lactone) complexes | 1.0 | 44 | Citations (PDF) |
| 736 | Dehydrogenation of lactones using benzeneseleninic anhydride. X-Ray crystal structure of 3β-acetoxy-14α-hydroxy-17a-oxa-D-homo-5α-androst-15-en-17-one | 1.0 | 19 | Citations (PDF) |
| 737 | Oxidation of benzylic hydrocarbons with benzeneseleninic anhydride and related reactions | 1.0 | 19 | Citations (PDF) |
| 738 | Thermal rearrangement reactions of tricarbonyliron lactone complexes | 1.0 | 16 | Citations (PDF) |
| 739 | The X-ray structure and absolute configuration of insect antifeedant clerodane diterpenoids from Teucrium africanum | 1.0 | 36 | Citations (PDF) |
| 740 | A practical catalytic method for the preparation of steroidal 1,4-dien-3-ones by oxygen atom transfer from iodoxybenzene to diphenyl diselenide | 1.0 | 58 | Citations (PDF) |
| 741 | An unexpected rearrangement of 4-alkylaminoindoles | 1.9 | 7 | Citations (PDF) |
| 742 | Synthesis of (cis-6-methyltetrahydropyran-2-yl)acetic acid involving the use of an organoselenium-mediated cyclization reaction | 1.9 | 24 | Citations (PDF) |
| 743 | A short syntesis of (±)-hirsutene involving the use of an organoselenium-mediated cyclization reaction | 1.9 | 32 | Citations (PDF) |
| 744 | Synthesis of polyoxygenated trans-decalins as potential insect antifeedants | 1.0 | 24 | Citations (PDF) |
| 745 | Synthesis of methyl-1,6-dioxaspiro[4,5]decanes using organoselenium mediated cyclization reactions | 1.4 | 45 | Citations (PDF) |
| 746 | A conformational study of elaiophylin by X-ray crystallography and difference 1H NMR methods; observation of a selective sign reversal of the nuclear overhauser effect | 1.4 | 35 | Citations (PDF) |
| 747 | Oxygen atom transfer from iodylbenzene to diphenyl diselenide - a convenient method for dehydrogenation of steroidal 3-ketones | 1.9 | 28 | Citations (PDF) |
| 748 | Preparation of lactones via tricarbonyliron–lactone complexes | 1.0 | 42 | Citations (PDF) |
| 749 | Synthesis of a trans-decalin as a potential insect antifeedant | 1.9 | 12 | Citations (PDF) |
| 750 | Synthesis of cinnamolide and polygodial | 1.9 | 24 | Citations (PDF) |
| 751 | On the reaction of thioacetals with sulphuryl chloride | 1.0 | 8 | Citations (PDF) |
| 752 | An intramolecular Diels-Alder approach to the synthesis of the right hand half of the ionophore antibiotic X-14547A | 1.4 | 17 | Citations (PDF) |
| 753 | The synthesis and Diels–Alder reactions of 2-prop-2-enylidene-1,3-dioxolan | 1.0 | 4 | Citations (PDF) |
| 754 | Experiments on the synthesis of tetracycline. Part 16. Improved photocyclic preparation of 12-keto-derivatives and their deprotection using benzeneseleninic anhydride | 1.0 | 6 | Citations (PDF) |
| 755 | Diaryl telluroxides as new mild oxidising reagents | 2.0 | 105 | Citations (PDF) |
| 756 | A convenient preparation of 2-haloenones from enones using phenylselenium halides | 1.4 | 45 | Citations (PDF) |
| 757 | Synthesis of euryfuran, valdiviolide, and confertifolin | 1.4 | 19 | Citations (PDF) |
| 758 | Cyclisation reactions of alkenyl β-ketoesters involving a novel phenylseleno group migration | 1.4 | 48 | Citations (PDF) |
| 759 | Synthesis of (±)warburganal | 1.4 | 16 | Citations (PDF) |
| 760 | Oxidation of phenols, pyrocatechols, and hydroquinones to ortho-quinones using benzeneseleninic anhydride | 1.0 | 50 | Citations (PDF) |
| 761 | Synthesis of substituted cis-decalins as potential insect antifeedants | 1.0 | 33 | Citations (PDF) |
| 762 | Removal of thioacetal protecting groups by benzeneseleninic anhydride | 1.0 | 29 | Citations (PDF) |
| 763 | Catalytic oxidation of thiocarbonyl compounds involving the use of 1,2-Dibrometatrachloroethane as a brominating reagent for diaryl teII species | 1.4 | 68 | Citations (PDF) |
| 764 | Chapter 13. Organosulphur, organoselenium, and organotellurium chemistry | 0.7 | 1 | Citations (PDF) |
| 765 | Oxidation of ketone and aldehyde hydrazones, oximes, and semicarbazones and of hydroxylamines and hydrazo-compounds, using benzeneseleninic anhydride | 1.0 | 56 | Citations (PDF) |
| 766 | Conversion of thiocarbonyl compounds into their corresponding oxoderivatives using benzeneseleninic anhydride | 1.0 | 48 | Citations (PDF) |
| 767 | Sulphuration of Electron-Rich Arenes with Sulphenamides and Aminosulphenyl Chlorides | 1.6 | 4 | Citations (PDF) |
| 768 | Selenium-mediated cyclization reactions of alkenyl-substituted β-ketoesters | 1.9 | 52 | Citations (PDF) |
| 769 | Dehydrogenation of steroidal and triterpenoid ketones using benzeneseleninic anhydride | 1.0 | 40 | Citations (PDF) |
| 770 | Thermal decomposition of tricarbonyliron lactone complexes | 1.9 | 9 | Citations (PDF) |
| 771 | New cyclization procedure for alkenyl-substituted β-dicarbonyl compounds using N-phenylselenophthalimide | 1.9 | 45 | Citations (PDF) |
| 772 | A new synthetic approach towards adriamycin | 1.0 | 8 | Citations (PDF) |
| 773 | Formation of β-lactams from tricarbonyliron lactone complexes | 1.9 | 22 | Citations (PDF) |
| 774 | Preparation of aldehydes and ketones by oxidation of benzylic hydrocarbons with benzeneseleninic anhydride | 1.4 | 25 | Citations (PDF) |
| 775 | Isolation, Characterisation and Oxidation of Isomeric Ferrelactone Complexes. | 2.1 | 13 | Citations (PDF) |
| 776 | Preparation of episulphides from alkenes via succinimide-N-sulphenyl chloride or phthalimide-N-sulphenyl chloride adducts | 1.0 | 48 | Citations (PDF) |
| 777 | Synthesis of a substituted cis-decalin as a potential insect antifeedant | 1.9 | 9 | Citations (PDF) |
| 778 | The crystal structure of 3-epicaryoptin and the reversal of the currently accepted absolute configuration of clerodin | 1.9 | 120 | Citations (PDF) |
| 779 | Bis(p-methoxyphenyl) telluroxide: a new, mild oxidising agent | 1.9 | 50 | Citations (PDF) |
| 780 | The formation of unusual sultones during the rearrangement reactions of bicyclic ketones | 1.4 | 5 | Citations (PDF) |
| 781 | Dehydrogenation of steroidal ketones using benzeneseleninic anhydride | 1.9 | 39 | Citations (PDF) |
| 782 | Oxidation of aldehyde hydrazones, hydrazo compounds, and hydroxylamines with benzeneseleninic anhydride | 1.9 | 29 | Citations (PDF) |
| 783 | Conversion of thiocarbonyl compounds into their corresponding oxo derivatives using benzeneseleninic anhydride | 1.9 | 25 | Citations (PDF) |
| 784 | Synthesis and reducibility of homo-2-methoxyazocines and their benzo-fused derivatives. An examination of heteroatomic influences on the possible generation of 9C-10.pi. homoaromatic dianions | 3.5 | 10 | Citations (PDF) |
| 785 | Thermal isomerization of homoazocines | 15.0 | 5 | Citations (PDF) |
| 786 | Oxidation of alcohols using benzeneseleninic anhydride | 1.9 | 57 | Citations (PDF) |
| 787 | Removal of 1,3-dithiolan protecting groups by benzeneseleninic anhydride | 1.9 | 20 | Citations (PDF) |
| 788 | X-Ray evidence for partial bonding between sulphur or selenium and oxygen in thio- and seleno-imines | 1.9 | 10 | Citations (PDF) |
| 789 | Regeneration of ketones from hydrazones, oximes, and semicarbazones by benzeneseleninic anhydride | 1.9 | 54 | Citations (PDF) |
| 790 | Preparation of phenylselenoimines from phenols using diphenylseleninic anhydride and hexamethyldisilazane | 1.9 | 22 | Citations (PDF) |
| 791 | Formation of lactones from dienes via iron carbonyl complexes | 1.9 | 8 | Citations (PDF) |
| 792 | Mechanism of the thermal decomposition of tetra-aryltellurium species | 1.9 | 36 | Citations (PDF) |
| 793 | The question of delocalization in "anchored" ions with potential trishomoaromatic character. 1. Reduction of tricyclo[5.4.1.04,12]dodeca-2,5,8,10-tetraene as a route to the 10.pi.11C dianion | 15.0 | 15 | Citations (PDF) |
| 794 | Experiments on the synthesis of tetracycline. Part 15. Oxidation of phenols and ring A model phenols to o-hydroxy-dienones with benzeneseleninic anhydride | 1.0 | 43 | Citations (PDF) |
| 795 | Reaction of tetracycline hydrochloride with N-chlorosuccinimide: X-ray crystal structure of the major product | 1.9 | 9 | Citations (PDF) |
| 796 | Formation of monohomocyclooctatetraene dianions in liquid ammonia. Analysis of the nucleophilic reactivity of the cyclononatrienyl anions generated upon solvent protonation | 15.0 | 11 | Citations (PDF) |
| 797 | Homotropylium-8-sulfinate complexes by antimony pentafluoride-promoted ring opening of 9-thiabicyclo[4.2.1]nona-2,4,7-triene and 9-thiabarbaralane 9,9-dioxides | 15.0 | 12 | Citations (PDF) |
| 798 | Oxidation of phenols to ortho-quinones using diphenylseleninic anhydride | 1.9 | 32 | Citations (PDF) |
| 799 | Unsaturated heterocyclic systems. XCII. Nitrogen analogs of 1,6-methano[12]annulene. Effect on valence tautomerism of the locus of aza substitution | 3.5 | 16 | Citations (PDF) |
| 800 | Synthesis, Chiroptical Properties, and Absolute Configuration of (+)-2,3-Dihydrotriquinacen-2-one. Effect of Rigid Triquinacene Geometry on the Inherently Dissymmetric Chromophore | 15.0 | 19 | Citations (PDF) |
| 801 | Tetracyanoethylene addition to iron tricarbonyl complexes of substituted cyclooctatetraenes. Regioselectivity considerations during formation of the 2,3,4,10-tetrahapto adducts | 15.0 | 35 | Citations (PDF) |
| 802 | The stability of NN-dialkylthiohydroxylamines | 1.9 | 17 | Citations (PDF) |
| 803 | Aryne chemistry. Part XXXV. Reactions of arynes with 1-aminocycloalkenes and hydrolyses of the adducts | 1.0 | 8 | Citations (PDF) |
| 804 | Rearrangement reactions of bicyclic systems. Part II. Rearrangements of 1-dimethylamino-5,6,7,8-tetrahalogeno-1,4-dihydro-1,4-ethenonaphthalene derivatives and the analogous 5,6,7,8-tetrafluoro-1,4-dihydro-N-methyl-1,4-iminonaphthalene in aqueous solutions | 1.0 | 10 | Citations (PDF) |
| 805 | Efficient synthesis of (-)-triquinacene-2-carboxylic acid | 15.0 | 19 | Citations (PDF) |
| 806 | Alkali metal reduction studies of cis- and trans-bicyclo[6.1.0]nona-2,4,6-trienes in liquid ammonia. Evidence for the high basicity of monohomocyclooctatetraene dianions | 15.0 | 19 | Citations (PDF) |
| 807 | Directed syntheses of the isomeric dimethylcyclooctatetraenes and a study of their polarographic and alkali metal reduction | 15.0 | 49 | Citations (PDF) |
| 808 | Aryne chemistry. Part XXXIV. Reactions of NN-dimethylarylamines with tetrahalogenobenzynes | 1.0 | 15 | Citations (PDF) |
| 809 | Rearrangement reactions of bicyclic systems. Part III. Acid-catalysed rearrangements of 1,4-dihydro-1-methoxy-1,4-ethenonaphthalene (1-methoxybenzobarrelene) and its 5,6,7,8-tetrahalogeno-derivatives | 1.0 | 11 | Citations (PDF) |
| 810 | Aryne chemistry. Part XXXIII. Reactions of tetrahalogenobenzynes with methoxyarenes and the photolysis and thermolysis of some of the products | 1.0 | 13 | Citations (PDF) |
| 811 | Rearrangement reactions of bicyclic systems. Part IV. Acid-catalysed rearrangements of 5,6,7,8-tetrafluoro-1,4-dihydro-1-methoxy-3,9-dimethyl-1,4-ethenonaphthalene (1-methoxy-3,5-dimethyltetrafluorobenzobarrelene) | 1.0 | 8 | Citations (PDF) |
| 812 | Mećhanistic dichotomy in cycloadditions to cyclooctatetraeneiron tricarbonyl. X-ray crystal structure analysis of the TCNE and CSI adducts | 1.4 | 21 | Citations (PDF) |
| 813 | N-alkylation of indole and pyrroles in dimethyl sulphoxide | 1.0 | 139 | Citations (PDF) |
| 814 | Rearrangement reactions of bicyclic systems. Part I. Synthesis of a model compound related to flavothebaone trimethyl ether. The abnormal ultraviolet absorption spectrum of flavothebaone and its trimethyl ether | 1.0 | 5 | Citations (PDF) |
| 815 | Thermal reactions of 1,4-bridged-1,2,3,4-tetrahydronaphthalene derivatives | 1.4 | 16 | Citations (PDF) |
| 816 | Multiple rearrangement reactions of 1-methoxybenzobarrelene (1,4-dihydro-1-methoxy-1,4-ethenonaphthalene) derivatives | 0.8 | 7 | Citations (PDF) |
| 817 | Acid-catalysed rearrangements of 3,5-dimethyl-1-methoxy-tetrafluorobenzobarrelene (5,6,7,8-tetrafluoro-1,4-dihydro-3,10-dimethyl-1-methoxy-1,4-ethenonaphthalene) | 0.8 | 4 | Citations (PDF) |
| 818 | Rearrangement reactions of 1-NN-dimethylaminobenzobenzobarrelene derivatives (benzobarrelene = 1,4-dihydro-1,4-ethenonaphthalene) | 0.8 | 2 | Citations (PDF) |
| 819 | Continuous Flow Techniques in the Total Synthesis of Jaspine B: Part II | 3.5 | 0 | Citations (PDF) |
