| 1 | Carbonyl group-assisted 1,3-amine addition to α,β-unsaturated aldehydes | 4.8 | 1 | Citations (PDF) |
| 2 | Photoredox-Catalyzed C(sp2)–H Bond Functionalization Reactions: A Short Account | 1.6 | 2 | Citations (PDF) |
| 3 | Uracil-Cu(<scp>i</scp>) catalyst: allylation of cyclopropanols with Morita–Baylis–Hillman alcohols under water-tolerant conditions | 7.1 | 9 | Citations (PDF) |
| 4 | Development and Applications of Water-Compatible Reactions: A Journey to Be Continued | 17.1 | 9 | Citations (PDF) |
| 5 | Silicon-Containing Thiol-Specific Bioconjugating Reagent | 15.0 | 26 | Citations (PDF) |
| 6 | Development and Applications of Water-Compatible Reactions: A Journey to Be Continued | 17.1 | 13 | Citations (PDF) |
| 7 | Triaryl Carbenium Ion Pair Mediated Electrocatalytic Benzylic C−H Oxygenation in Air | 14.4 | 18 | Citations (PDF) |
| 8 | Triaryl Carbenium Ion Pair Mediated Electrocatalytic Benzylic C−H Oxygenation in Air | 1.4 | 1 | Citations (PDF) |
| 9 | Photocatalytic Decarboxylative Allylation of α-Amino Acids and Peptides under Metal-Free Conditions | 4.8 | 6 | Citations (PDF) |
| 10 | β-Silyl alkynoates: Versatile reagents for biocompatible and selective amide bond formation | 11.0 | 6 | Citations (PDF) |
| 11 | Catalyst-Free Reactions under Biocompatible Conditions | 1.6 | 6 | Citations (PDF) |
| 12 | Metal-free access to β-carbolines via single-electron transfer catalyzed by a triaryl carbenium ion pair | 4.9 | 21 | Citations (PDF) |
| 13 | Ionogels: recent advances in design, material properties and emerging biomedical applications | 37.8 | 255 | Citations (PDF) |
| 14 | Alkynone β-trifluoroborates: A new class of amine-specific biocompatible click reagents | 11.0 | 20 | Citations (PDF) |
| 15 | Regioselective and Geometrically Controlled Heck 1,1-Diarylation of Unactivated Aliphatic Alkenes | 4.8 | 11 | Citations (PDF) |
| 16 | A Rare Earth Metal Catalyzed Aerobic Dehydrogenation of <i>N</i>-Heterocycles | 4.8 | 9 | Citations (PDF) |
| 17 | Organophotoredox-Catalyzed Intermolecular Formal Grob Fragmentation of Cyclic Alcohols with Activated Allylic Acetates | 4.8 | 9 | Citations (PDF) |
| 18 | Fluoroalkylation of Activated Allylic Acetates through Radical–Radical Coupling: Organophotoredox/DABCO Catalytic System | 4.8 | 13 | Citations (PDF) |
| 19 | Thiol‐Specific Silicon‐Containing Conjugating Reagent: <i>β</i>‐Silyl Alkynyl Carbonyl Compounds | 14.4 | 16 | Citations (PDF) |
| 20 | Calcium-catalyzed dehydrative allylation of P-ylides and sequential Wittig reaction for streamlined access to versatile 1,4-dienes | 2.4 | 3 | Citations (PDF) |
| 21 | Recent advances in ligand-enabled palladium-catalyzed divergent synthesis | 2.6 | 22 | Citations (PDF) |
| 22 | Silver-mediated synthesis of 1,4-dihydropyridine sulfones <i>via</i> [4 + 2] cyclization of <i>N</i>-allenylsulfonamides and enaminones with a 1,3-sulfonyl shift | 4.4 | 7 | Citations (PDF) |
| 23 | Oxidative Amination of Aldehydes with Amines into α-Amino Ketones | 4.8 | 10 | Citations (PDF) |
| 24 | Sulfination of Unactivated Allylic Alcohols via Sulfinate–Sulfone Rearrangement | 4.8 | 5 | Citations (PDF) |
| 25 | Metal-Free Access to (<i>Spirocyclic</i>)Tetrahydro-β-carbolines in Water Using an Ion-Pair as a Superacidic Precatalyst | 12.4 | 26 | Citations (PDF) |
| 26 | Catalyst-free C–N bond formation under biocompatible reaction conditions | 9.1 | 15 | Citations (PDF) |
| 27 | BF<sub>3</sub>-promoted reactions of α-amino acetals with alkynes to 2,5-disubstituted pyrroles | 4.4 | 6 | Citations (PDF) |
| 28 | Catalyst‐ and Metal‐Free Photo‐Oxidative Coupling of Thiols with BrCCl<sub>3</sub> | 2.3 | 13 | Citations (PDF) |
| 29 | Dehydrative Cross-Coupling for C–N Bond Construction under Transition-Metal-Free Conditions | 4.8 | 5 | Citations (PDF) |
| 30 | Metal-free synthesis of 3,3′-bisindolylmethanes in water using Ph<sub>3</sub>C<sup>+</sup>[B(C<sub>6</sub>F<sub>5</sub>)<sub>4</sub>]<sup>−</sup> as the pre-catalyst | 4.4 | 22 | Citations (PDF) |
| 31 | Development of catalyst-free carbon-sulfur bond formation reactions under aqueous media and their applications | 4.8 | 25 | Citations (PDF) |
| 32 | Recent Advances in Alkenyl sp<sup>2</sup> C–H and C–F Bond Functionalizations: Scope, Mechanism, and Applications | 52.7 | 209 | Citations (PDF) |
| 33 | Triaryl Carbonium Ion-Pair-Mediated Cooperative Aerobic Dehydrogenation of N-Heterocycles | 12.4 | 22 | Citations (PDF) |
| 34 | Aqueous C–H aminomethylation of phenols by iodine catalysis | 3.4 | 7 | Citations (PDF) |
| 35 | One-Pot and Unsymmetrical Bis-Allylation of Malononitrile with Conjugated Dienes and Allylic Alcohols | 4.8 | 5 | Citations (PDF) |
| 36 | Access to multi-functionalized oxazolines via silver-catalyzed heteroannulation of enamides with sulfoxonium ylides | 7.5 | 18 | Citations (PDF) |
| 37 | Iridium-promoted deoxyglycoside synthesis: stereoselectivity and mechanistic insight | 7.1 | 19 | Citations (PDF) |
| 38 | Additive-free <i>N</i>-methylation of amines with methanol over supported iridium catalyst | 4.0 | 26 | Citations (PDF) |
| 39 | Photoinitiated stereoselective direct C(sp<sup>2</sup>)–H perfluoroalkylation and difluoroacetylation of enamides | 4.4 | 49 | Citations (PDF) |
| 40 | Visible light-induced mono-bromination of arenes with BrCCl<sub>3</sub> | 3.4 | 27 | Citations (PDF) |
| 41 | Copper-Catalyzed Meta-Selective Arylation of Phenol Derivatives: An Easy Access to <i>m</i>-Aryl Phenols | 12.4 | 25 | Citations (PDF) |
| 42 | Targeting RNA editing of antizyme inhibitor 1: A potential oligonucleotide-based antisense therapy for cancer | 10.4 | 26 | Citations (PDF) |
| 43 | Direct Synthesis of α-Amino Nitriles from Sulfonamides via Base-Mediated C–H Cyanation | 4.8 | 8 | Citations (PDF) |
| 44 | Visible-Light-Induced Trifluoromethylation of Allylic Alcohols | 4.8 | 28 | Citations (PDF) |
| 45 | Water-Tolerant <i>ortho</i>-Acylation of Phenols | 4.8 | 11 | Citations (PDF) |
| 46 | Intramolecular Alkene–Alkene Coupling via Rh(III)-Catalyzed Alkenyl sp<sup>2</sup> C–H Functionalization: Divergent Pathways to Indene or α-Naphthol Derivatives | 12.4 | 12 | Citations (PDF) |
| 47 | Metal-free C(sp<sup>3</sup>)–H functionalization of sulfonamides<i>via</i>strain-release rearrangement | 7.1 | 10 | Citations (PDF) |
| 48 | Synthesis of Vinylic Sulfones in Aqueous Media | 4.8 | 38 | Citations (PDF) |
| 49 | Readily useable bulk phenoxazine-based covalent organic framework cathode materials with superior kinetics and high redox potentials | 9.3 | 36 | Citations (PDF) |
| 50 | Dehydrative allylation of P–H species under metal-free conditions | 9.1 | 25 | Citations (PDF) |
| 51 | Practical allylation with unactivated allylic alcohols under mild conditions | 4.4 | 8 | Citations (PDF) |
| 52 | Recent developments in chemical conjugation strategies targeting native amino acids in proteins and their applications in antibody–drug conjugates | 7.1 | 124 | Citations (PDF) |
| 53 | Intermolecular Reductive Heck Reaction of Unactivated Aliphatic Alkenes with Organohalides | 4.8 | 45 | Citations (PDF) |
| 54 | Alkaline-Earth Metal Catalyzed Dehydrative Allylic Alkylation | 4.8 | 23 | Citations (PDF) |
| 55 | Dichloroacetophenone Derivatives: A Class of Bioconjugation Reagents for Disulfide Bridging | 4.8 | 17 | Citations (PDF) |
| 56 | Hydrazine as Facile Nitrogen Source for Direct Synthesis of Amines over a Supported Pt Catalyst | 6.9 | 18 | Citations (PDF) |
| 57 | Regio- and stereoselective C(sp<sup>2</sup>)–H acylation of enamides with aldehydes <i>via</i> transition-metal-free photoredox catalysis | 9.1 | 49 | Citations (PDF) |
| 58 | Stereoselective Synthesis of Vinylcyclopropa[<i>b</i>]indolines via a Rh-Migration Strategy | 4.8 | 19 | Citations (PDF) |
| 59 | Palladium-Catalyzed Intermolecular Polarity-Mismatched Addition of Unactivated Alkyl Radicals to Unactivated Alkenes | 12.4 | 43 | Citations (PDF) |
| 60 | Macrolactam Synthesis via Ring-Closing Alkene–Alkene Cross-Coupling Reactions | 4.8 | 14 | Citations (PDF) |
| 61 | Buckyball-Based Spherical Display of Crown Ethers for <i>De Novo</i> Custom Design of Ion Transport Selectivity | 15.0 | 75 | Citations (PDF) |
| 62 | Decarboxylative C–H Alkylation of Heteroarene <i>N</i>-Oxides by Visible Light/Copper Catalysis | 4.8 | 29 | Citations (PDF) |
| 63 | Visible-Light-Induced Regio- and Stereoselective C(sp<sup>2</sup>)–H Trifluoroethylation of Enamides with 2,2,2-Trifluoroethyl Iodide | 4.8 | 43 | Citations (PDF) |
| 64 | An efficient method for the synthesis of 2-pyridones <i>via</i> C–H bond functionalization | 3.4 | 25 | Citations (PDF) |
| 65 | Cancer Biomarker-Triggered Disintegrable DNA Nanogels for Intelligent Drug Delivery | 8.7 | 49 | Citations (PDF) |
| 66 | Directed Palladium(II)-Catalyzed Intermolecular Anti-Markovnikov Hydroarylation of Unactivated Alkenes with (Hetero)arylsilanes | 4.8 | 18 | Citations (PDF) |
| 67 | Palladium-Catalyzed <i>anti</i>-Michael Reductive Heck Reaction of α,β-Unsaturated Esters | 12.4 | 47 | Citations (PDF) |
| 68 | Reciprocal-Activation Strategy for Allylic Sulfination with Unactivated Allylic Alcohols | 4.8 | 30 | Citations (PDF) |
| 69 | Direct Hiyama Cross-Coupling of (Hetero)arylsilanes with C(sp<sup>2</sup>)–H Bonds Enabled by Cobalt Catalysis | 4.8 | 38 | Citations (PDF) |
| 70 | 2<i>H</i>-Azirines as Potential Bifunctional Chemical Linkers of Cysteine Residues in Bioconjugate Technology | 4.8 | 35 | Citations (PDF) |
| 71 | Cleavage and Reassembly C≡C Bonds of Ynones to Access Highly Functionalized Ketones | 12.4 | 22 | Citations (PDF) |
| 72 | Selective Dehydrogenative Acylation of Enamides with Aldehydes Leading to Valuable β-Ketoenamides | 4.8 | 31 | Citations (PDF) |
| 73 | Stereoselective synthesis of trifluoromethyl-substituted 2<i>H</i>-furan-amines from enaminones | 3.4 | 43 | Citations (PDF) |
| 74 | Dehydrative Cross-Coupling of Allylic Alcohols with Alkynes | 4.8 | 31 | Citations (PDF) |
| 75 | A Ba/Pd Catalytic System Enables Dehydrative Cross-Coupling and Excellent E-Selective Wittig Reactions | 4.8 | 9 | Citations (PDF) |
| 76 | The ruthenium-catalyzed C–H functionalization of enamides with isocyanates: easy entry to pyrimidin-4-ones | 3.4 | 35 | Citations (PDF) |
| 77 | Palladium-Catalyzed Cycloaromatization/Alkylation of o-(Alkynyl)styrenes | 3.5 | 6 | Citations (PDF) |
| 78 | α-Amino Acetal: A Synthetic Intermediate for the Construction of Aza-Polycycles | 4.8 | 12 | Citations (PDF) |
| 79 | Photoredox-catalyzed stereoselective alkylation of enamides with <i>N</i>-hydroxyphthalimide esters <i>via</i> decarboxylative cross-coupling reactions | 7.1 | 87 | Citations (PDF) |
| 80 | Iron(0)-Mediated Reformatsky Reaction for the Synthesis of β-Hydroxyl Carbonyl Compounds | 4.8 | 24 | Citations (PDF) |
| 81 | Regioselective and Stereoselective Difluoromethylation of Enamides with Difluoromethyltriphenylphosphonium Bromide via Photoredox Catalysis | 4.8 | 80 | Citations (PDF) |
| 82 | Iron-Catalyzed Carbamoylation of Enamides with Formamides as a Direct Approach to <i>N</i>-Acyl Enamine Amides | 12.4 | 57 | Citations (PDF) |
| 83 | Chemo‐ and Regioselective Ring Construction Driven by Visible‐Light Photoredox Catalysis: an Access to Fluoroalkylated Oxazolidines Featuring an All‐Substituted Carbon Stereocenter | 3.8 | 25 | Citations (PDF) |
| 84 | Synthesis of Functionalized α‐Vinyl Aldehydes from Enaminones | 14.4 | 60 | Citations (PDF) |
| 85 | Synthesis of Functionalized α‐Vinyl Aldehydes from Enaminones | 1.4 | 4 | Citations (PDF) |
| 86 | Copper‐Catalyzed Asymmetric Silylation of Propargyl Dichlorides: Access to Enantioenriched Functionalized Allenylsilanes | 14.4 | 55 | Citations (PDF) |
| 87 | Transition‐Metal‐Free Deaminative Vinylation of Alkylamines | 3.8 | 35 | Citations (PDF) |
| 88 | Calcium-catalyzed regioselective dehydrative cross-coupling of propargylic alcohols with 1,3-dicarbonyl compounds | 9.1 | 19 | Citations (PDF) |
| 89 | MoS2-nanosheet-decorated C-N/Co4S3 nanorod hybrid as a bifunctional electrocatalyst | 3.9 | 15 | Citations (PDF) |
| 90 | Selectfluor™-catalyzed oxidative cyclization of ynamides enables facile synthesis of oxazolidine-2,4-diones | 4.4 | 14 | Citations (PDF) |
| 91 | Stereoselective C(sp<sup>2</sup>)–H Alkylation of Enamides with Unactivated Aliphatic Carboxylic Acids via Decarboxylative Cross-Coupling Reactions | 4.8 | 52 | Citations (PDF) |
| 92 | Metallic salt-catalyzed direct indium insertion into alkyl iodides and their applications in cross-coupling reactions | 4.4 | 17 | Citations (PDF) |
| 93 | Reactions of 5-Aminoisoxazoles with α-Diazocarbonyl Compounds: Wolff Rearrangement vs N–H Insertion | 3.5 | 13 | Citations (PDF) |
| 94 | Transition-Metal-Catalyzed Alkenyl sp2 C–H Activation: A Short Account | 2.3 | 53 | Citations (PDF) |
| 95 | Cu(OTf)<sub>2</sub>-mediated C(sp<sup>2</sup>)–H arylsulfonylation of enamides <i>via</i> the insertion of sulfur dioxide | 4.4 | 81 | Citations (PDF) |
| 96 | Copper-catalyzed regiodivergent 1,4- and 1,6-conjugate silyl addition to diendioates: access to functionalized allylsilanes | 2.6 | 15 | Citations (PDF) |
| 97 | Manganese-Catalyzed Ring-Opening Coupling Reactions of Cyclopropanols with Enones | 4.8 | 49 | Citations (PDF) |
| 98 | Allylic Phosphorus Ylides Directly Generated from Alcohols with Water as the Only Byproduct | 4.8 | 23 | Citations (PDF) |
| 99 | Reduced graphene oxide-supported cobalt oxide decorated N-doped graphitic carbon for efficient bifunctional oxygen electrocatalysis | 4.4 | 44 | Citations (PDF) |
| 100 | Palladium-Catalyzed Dialkylation of C–C Triple Bonds: Access to Multi-Functionalized Indenes | 4.8 | 17 | Citations (PDF) |
| 101 | Palladium-Catalyzed Cascade Intramolecular Cyclization and Allylation of Enynoates with Allylic Alcohols | 3.5 | 19 | Citations (PDF) |
| 102 | Site-selective C(sp<sup>3</sup>)–H amination of thioamide with anthranils under Cp*Co<sup>III</sup>catalysis | 3.4 | 49 | Citations (PDF) |
| 103 | Direct C(<i>sp</i><sup>2</sup>)‐H Arylsulfonylation of Enamides <i>via</i> Iridium(III)‐Catalyzed Insertion of Sulfur Dioxide with Aryldiazonium Tetrafluoroborates | 3.8 | 78 | Citations (PDF) |
| 104 | Iron-mediated highly diastereoselective allylation of carbonyl compounds with cyclic allylic halides | 4.4 | 19 | Citations (PDF) |
| 105 | Regioselective C–H Amidation of (Alkyl)arenes by Iron(II) Catalysis | 4.8 | 14 | Citations (PDF) |
| 106 | Palladium(II)-Catalyzed Stereospecific Alkenyl C–H Bond Alkylation of Allylamines with Alkyl Iodides | 12.4 | 40 | Citations (PDF) |
| 107 | Lead-Mediated Highly Diastereoselective Allylation of Aldehydes with Cyclic Allylic Halides | 3.5 | 24 | Citations (PDF) |
| 108 | Supported Iridium Catalyst for the Green Synthesis of 3,3′-Bis(indolyl)methanes Using Methanol As the Bridging Methylene Source | 6.9 | 43 | Citations (PDF) |
| 109 | Divergent Protosilylation and Protoborylation of Polar Enynes | 4.8 | 27 | Citations (PDF) |
| 110 | Divergent C–H Oxidative Radical Functionalization of Olefins to Install Tertiary Alkyl Motifs Enabled by Copper Catalysis | 4.8 | 32 | Citations (PDF) |
| 111 | Cobalt-Catalyzed N–O and C–C Bond Cleavage in 1,2-Oxazetidines: Solvent-Controlled C–H Aminomethylation and Hydroxymethylation of Heteroarenes | 4.8 | 40 | Citations (PDF) |
| 112 | Bismuth‐Mediated Diastereoselective Allylation Reaction of Carbonyl Compounds with Cyclic Allylic Halides or Cinnamyl Halide | 3.8 | 29 | Citations (PDF) |
| 113 | Oxidant-directed chemoselective sulfonylation and sulfonyloximation of alkenes <i>via</i> cleaving the C–S bond in TosMIC | 4.4 | 46 | Citations (PDF) |
| 114 | Formal synthesis of chelamidine alkaloids and their derivatives | 3.4 | 7 | Citations (PDF) |
| 115 | Combining Fluoroalkylation and Defluorination to Enable Formal [3 + 2 + 1] Heteroannulation by Using Visible-Light Photoredox Organocatalysis | 4.8 | 49 | Citations (PDF) |
| 116 | Hoveyda–Grubbs II Catalyst: A Useful Catalyst for One-Pot Visible-Light-Promoted Ring Contraction and Olefin Metathesis Reactions | 4.8 | 35 | Citations (PDF) |
| 117 | Water-promoted C-S bond formation reactions | 13.9 | 118 | Citations (PDF) |
| 118 | Macrolide Synthesis through Intramolecular Oxidative Cross‐Coupling of Alkenes | 1.4 | 14 | Citations (PDF) |
| 119 | Copper-catalyzed three-component cyclization of amidines, styrenes, and fluoroalkyl halides for the synthesis of modular fluoroalkylated pyrimidines | 3.4 | 60 | Citations (PDF) |
| 120 | Palladium-catalyzed silaborative carbocyclizations of 1,6-diynes | 3.4 | 18 | Citations (PDF) |
| 121 | Highly Site-Selective Metal-Free C–H Acyloxylation of Stable Enamines | 4.8 | 68 | Citations (PDF) |
| 122 | Pyrroline Synthesis via Visible‐Light‐Promoted Hydroimination of Unactivated Alkenes with <i>N</i>,<i>N′</i>‐Dimethylpropylene Urea as <i>H</i>‐Donor | 3.8 | 38 | Citations (PDF) |
| 123 | Directing Group Participated Benzylic C(sp<sup>3</sup>)–H/C(sp<sup>2</sup>)–H Cross-Dehydrogenative Coupling (CDC): Synthesis of Azapolycycles | 4.8 | 33 | Citations (PDF) |
| 124 | Indium(III)‐Catalyzed Hydration and Hydroalkoxylation of α,β‐Unsaturated Ketones in Aqueous Media | 3.8 | 31 | Citations (PDF) |
| 125 | Rh-Catalyzed C–H bond alkylation of indoles with α,α-difluorovinyl tosylate <i>via</i> indolyl group migration | 3.4 | 38 | Citations (PDF) |
| 126 | Catalytically Asymmetric Synthesis of 1,3-Bis(silyl)propenes via Copper-Catalyzed Double Proto-Silylations of Polar Enynes | 12.4 | 29 | Citations (PDF) |
| 127 | Synthesis of Alkyl Indium Reagents by Using Unactivated Alkyl Chlorides and Their Applications in Palladium-Catalyzed Cross-Coupling Reactions with Aryl Halides | 4.8 | 42 | Citations (PDF) |
| 128 | Iridium(III)‐Catalyzed Selective and Mild C‐H Amidation of Cyclic <i>N</i>‐Sulfonyl Ketimines with Organic Azides | 3.8 | 25 | Citations (PDF) |
| 129 | Macrolide Synthesis through Intramolecular Oxidative Cross‐Coupling of Alkenes | 14.4 | 96 | Citations (PDF) |
| 130 | Selective Binding to mRNA Duplex Regions by Chemically Modified Peptide Nucleic Acids Stimulates Ribosomal Frameshifting | 2.4 | 36 | Citations (PDF) |
| 131 | Recent Advances in Radical-Initiated C(sp<sup>3</sup>)–H Bond Oxidative Functionalization of Alkyl Nitriles | 12.4 | 203 | Citations (PDF) |
| 132 | Polycyclic heteroaromatic ring construction driven by silver/cobalt co-catalyzed desulfonylative and defluorinative fragment-recombination of enol nonaflates with amidines | 3.4 | 21 | Citations (PDF) |
| 133 | Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C–H Bond Functionalization | 4.8 | 69 | Citations (PDF) |
| 134 | Palladium-Catalyzed One-Pot Highly Regioselective 6-<i>Endo</i> Cyclization and Alkylation of Enynoates: Synthesis of 2-Alkanone Pyrones | 3.5 | 18 | Citations (PDF) |
| 135 | Barium-catalyzed C–OH/P–H dehydrative cross-coupling for C–P bond construction | 3.4 | 33 | Citations (PDF) |
| 136 | Copper-Catalyzed Stereo- and Enantioselective 1,4-Protosilylation of <i>α,β</i>-Unsaturated Ketimines To Synthesize Functionalized Allylsilanes | 12.4 | 39 | Citations (PDF) |
| 137 | Bronsted Acid/Organic Photoredox Cooperative Catalysis: Easy Access to Tri- and Tetrasubstituted Alkenylphosphorus Compounds from Alcohols and P–H Species | 4.8 | 42 | Citations (PDF) |
| 138 | Copper-Catalyzed Dehydrogenative Diels–Alder Reaction | 4.8 | 31 | Citations (PDF) |
| 139 | Regioselective Copper-Catalyzed Oxidative Coupling of α-Alkylated Styrenes with Tertiary Alkyl Radicals | 4.8 | 32 | Citations (PDF) |
| 140 | In(III)-TMSBr-Catalyzed Cascade Reaction of Diarylalkynes with Acrylates for the Synthesis of Aryldihydronaphthalene Derivatives | 4.3 | 5 | Citations (PDF) |
| 141 | Direct Substitution of Secondary and Tertiary Alcohols To Generate Sulfones under Catalyst- and Additive-Free Conditions | 4.8 | 37 | Citations (PDF) |
| 142 | Chromium(III)-Catalyzed Addition of Water and Alcohol to α,β-Unsaturated Ketones for the Synthesis of β-Hydroxyl and β-Alkoxyl Ketones in Aqueous Media | 3.5 | 20 | Citations (PDF) |
| 143 | Visible Light‐Mediated Trifluoromethylation of Fluorinated Alkenes via C−F Bond Cleavage | 3.8 | 99 | Citations (PDF) |
| 144 | Bioinspired Deamination of <i>α</i>‐Amino Acid Derivatives Catalyzed by a Palladium/Nickel Complex | 3.8 | 11 | Citations (PDF) |
| 145 | Palladium-Catalyzed Regioselective Olefination of <i>O</i>-Acetyl Cyanohydrins | 3.5 | 12 | Citations (PDF) |
| 146 | Regioselective Formal [4 + 2] Cycloadditions of Enaminones with Diazocarbonyls through Rh<sup>III</sup>-Catalyzed C–H Bond Functionalization | 4.8 | 35 | Citations (PDF) |
| 147 | Palladium-Catalyzed Regiocontrollable Reductive Heck Reaction of Unactivated Aliphatic Alkenes | 15.0 | 131 | Citations (PDF) |
| 148 | C–F Bond Cleavage Enabled Redox-Neutral [4+1] Annulation via C–H Bond Activation | 15.0 | 149 | Citations (PDF) |
| 149 | Palladium-Catalyzed Direct Intramolecular C–N Bond Formation: Access to Multisubstituted Dihydropyrroles | 4.8 | 31 | Citations (PDF) |
| 150 | The C–OH/P–H dehydrative cross-coupling for the construction of the P–C bond under metal-free conditions | 9.1 | 42 | Citations (PDF) |
| 151 | Rhodium(<scp>iii</scp>)-catalyzed directed C–H benzylation and allylation of indoles with organosilicon reagents | 4.4 | 28 | Citations (PDF) |
| 152 | Copper-catalyzed trifluoromethylation of styrene derivatives with CF<sub>3</sub>SO<sub>2</sub>Na | 4.4 | 51 | Citations (PDF) |
| 153 | Switchable C–H Functionalization of <i>N</i>-Tosyl Acrylamides with Acryloylsilanes | 4.8 | 39 | Citations (PDF) |
| 154 | Direct coupling of sp<sup>3</sup> carbon of alkanes with α,β-unsaturated carbonyl compounds using a copper/hydroperoxide system | 4.4 | 30 | Citations (PDF) |
| 155 | Chelation versus Non‐Chelation Control in the Stereoselective Alkenyl sp<sup>2</sup> C−H Bond Functionalization Reaction | 1.4 | 13 | Citations (PDF) |
| 156 | Chelation versus Non‐Chelation Control in the Stereoselective Alkenyl sp<sup>2</sup> C−H Bond Functionalization Reaction | 14.4 | 85 | Citations (PDF) |
| 157 | Redox‐Neutral Rhodium‐Catalyzed [4+1] Annulation through Formal Dehydrogenative Vinylidene Insertion | 6.2 | 55 | Citations (PDF) |
| 158 | Directed C–C bond cleavage of a cyclopropane intermediate generated from<i>N</i>-tosylhydrazones and stable enaminones: expedient synthesis of functionalized 1,4-ketoaldehydes | 3.4 | 53 | Citations (PDF) |
| 159 | Iron-catalyzed peroxidation–carbamoylation of alkenes with hydroperoxides and formamides <i>via</i> formyl C(sp<sup>2</sup>)–H functionalization | 3.4 | 38 | Citations (PDF) |
| 160 | An iron-catalyzed hydroalkylation reaction of α,β-unsaturated ketones with ethers | 3.4 | 20 | Citations (PDF) |
| 161 | Copper-Catalyzed Silylperoxidation Reaction of α,β-Unsaturated Ketones, Esters, Amides, and Conjugated Enynes | 12.4 | 86 | Citations (PDF) |
| 162 | Lewis Acid-Catalyzed Selective [2 + 2]-Cycloaddition and Dearomatizing Cascade Reaction of Aryl Alkynes with Acrylates | 15.0 | 71 | Citations (PDF) |
| 163 | Copper-catalyzed silylation reactions of propargyl epoxides: easy access to 2,3-allenols and stereodefined alkenes | 3.4 | 38 | Citations (PDF) |
| 164 | Nonconventional difluoroalkylation of C(sp<sup>2</sup>)–H bonds through hydroarylation | 3.4 | 44 | Citations (PDF) |
| 165 | Palladium-Catalyzed Direct C–H Trifluoroethylation of Aromatic Amides | 4.8 | 43 | Citations (PDF) |
| 166 | Photoredox Catalysis Induced Bisindolylation of Ethers/Alcohols via Sequential C–H and C–O Bond Cleavage | 4.8 | 53 | Citations (PDF) |
| 167 | Palladium‐Catalyzed Fluoroarylation of <i>gem</i>‐Difluoroalkenes | 14.4 | 109 | Citations (PDF) |
| 168 | Palladium‐Catalyzed Fluoroarylation of
gem
‐Difluoroalkenes | 1.4 | 22 | Citations (PDF) |
| 169 | Manganese-catalyzed synthesis of monofluoroalkenes via C–H activation and C–F cleavage | 3.4 | 114 | Citations (PDF) |
| 170 | Transition metal-catalyzed cross-coupling reactions using organoindium reagents | 37.8 | 118 | Citations (PDF) |
| 171 | Palladium‐Catalyzed C–S Bond Formation of Stable Enamines with Arene/Alkanethiols: Highly Regioselective Synthesis of β‐Amino Sulfides | 2.3 | 56 | Citations (PDF) |
| 172 | Anomalous Reactivity and Selectivity in the Intermolecular Diels–Alder Reactions of Multisubstituted Acyclic Dienes with Geometrical Isomers of Enals | 4.8 | 7 | Citations (PDF) |
| 173 | Chelation-Assisted Rhodium-Catalyzed Direct Amidation with Amidobenziodoxolones: C(sp<sup>2</sup>)–H, C(sp<sup>3</sup>)–H, and Late-Stage Functionalizations | 12.4 | 110 | Citations (PDF) |
| 174 | Aerobic Copper Catalysis for Tandem Oxy‐<i>N</i>‐alkenylation of [1,2,3]Triazolo[1,5‐<i>a</i>]pyridines | 3.8 | 7 | Citations (PDF) |
| 175 | F<sup>–</sup> Nucleophilic-Addition-Induced Allylic Alkylation | 15.0 | 122 | Citations (PDF) |
| 176 | Copper-catalyzed oxyamination of electron-deficient alkenes with N-acyloxyamines | 3.4 | 42 | Citations (PDF) |
| 177 | Visible-Light-Promoted Carboimination of Unactivated Alkenes for the Synthesis of Densely Functionalized Pyrroline Derivatives | 12.4 | 132 | Citations (PDF) |
| 178 | Stereoselective Synthesis of <i>cis</i>‐2,5‐Disubstituted Pyrrolidines via Copper‐Catalyzed Cyclization of Alkenes | 6.5 | 1 | Citations (PDF) |
| 179 | Incorporating a guanidine-modified cytosine base into triplex-forming PNAs for the recognition of a C-G pyrimidine–purine inversion site of an RNA duplex | 15.7 | 39 | Citations (PDF) |
| 180 | Rh<sup>III</sup>‐Catalyzed Hydroarylation of Internal Alkynes through C−H Bond Activation | 2.3 | 19 | Citations (PDF) |
| 181 | Asymmetric P−C Bond Formation: Diastereoselective Synthesis of Adjacent P,C‐Stereogenic Allylic Phosphorus Compounds | 3.0 | 15 | Citations (PDF) |
| 182 | Palladium-catalyzed silylation reaction between benzylic halides and silylboronate | 3.4 | 44 | Citations (PDF) |
| 183 | Palladium-catalyzed cross-coupling of enamides with sterically hindered α-bromocarbonyls | 3.4 | 80 | Citations (PDF) |
| 184 | Synthesis and Crystal Structure of Highly Strained [4]Cyclofluorene: Green-Emitting Fluorophore | 4.8 | 78 | Citations (PDF) |
| 185 | Selective Dealkylation of Alkyl Aryl Ethers | 2.3 | 25 | Citations (PDF) |
| 186 | Selective Alkenylation and Hydroalkenylation of Enol Phosphates through Direct CH Functionalization | 1.4 | 17 | Citations (PDF) |
| 187 | Selective Alkenylation and Hydroalkenylation of Enol Phosphates through Direct CH Functionalization | 14.4 | 103 | Citations (PDF) |
| 188 | Highly Enantioselective and <i>Anti</i>-Diastereoselective Catalytic Intermolecular Glyoxylate–Ene Reactions: Effect of the Geometrical Isomers of Alkenes | 4.8 | 17 | Citations (PDF) |
| 189 | Copper-Catalyzed Vicinal Oxyazidation and Diazidation of Styrenes under Mild Conditions: Access to Alkyl Azides | 4.8 | 123 | Citations (PDF) |
| 190 | Synthesis of Highly Substituted Racemic and Enantioenriched Allenylsilanes via Copper-Catalyzed Hydrosilylation of (<i>Z</i>)-2-Alken-4-ynoates with Silylboronate | 15.0 | 140 | Citations (PDF) |
| 191 | Pd-Catalyzed Intramolecular C–N Bond Cleavage, 1,4-Migration, sp<sup>3</sup> C–H Activation, and Heck Reaction: Four Controllable Diverse Pathways Depending on the Judicious Choice of the Base and Ligand | 15.0 | 161 | Citations (PDF) |
| 192 | Copper‐Catalyzed Enantioselective Conjugate Addition of Grignard Reagents to Methyl 4,4,4‐Trifluorocrotonate: Synthesis of Enantioenriched Trifluoromethylated Compounds | 3.0 | 16 | Citations (PDF) |
| 193 | Bifunctional Amino Sulfonohydrazide Catalyzed Direct Asymmetric Mannich Reaction of Cyclic Ketimines with Ketones: Highly Diastereo- and Enantioselective Construction of Quaternary Carbon Stereocenters | 4.8 | 72 | Citations (PDF) |
| 194 | Stereo- and Chemoselective Cross-Coupling between Two Electron-Deficient Acrylates: An Efficient Route to (<i>Z</i>,<i>E</i>)-Muconate Derivatives | 15.0 | 164 | Citations (PDF) |
| 195 | Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides | 3.4 | 11 | Citations (PDF) |
| 196 | Rhodium-catalysed C(sp2)–C(sp2) bond formation via C–H/C–F activation | 13.9 | 247 | Citations (PDF) |
| 197 | Divergent Functionalization of Indoles with Acryloyl Silanes via Rhodium-Catalyzed C–H Activation | 4.8 | 82 | Citations (PDF) |
| 198 | Palladium-Catalyzed Intermolecular Oxyarylation of Vinylacetates with Retention of an Alkenyl Moiety | 4.8 | 8 | Citations (PDF) |
| 199 | Expedient Synthesis of Pyrroloquinolinones by Rh-Catalyzed Annulation of<i>N</i>-Carbamoyl Indolines with Alkynes through a Directed C–H Functionalization/C–N Cleavage Sequence | 4.8 | 88 | Citations (PDF) |
| 200 | Palladium-Catalyzed Difunctionalization of Internal Alkynes via Highly Regioselective 6-<i>Endo</i> Cyclization and Alkenylation of Enynoates: Synthesis of Multisubstituted Pyrones | 4.8 | 51 | Citations (PDF) |
| 201 | C<sub>sp<sup>3</sup></sub>–C<sub>sp<sup>3</sup></sub>Bond Cleavage in the Palladium-Catalyzed Aminohydroxylation of Allylic Hydrazones Using Atmospheric Oxygen as the Sole Oxidant | 4.8 | 24 | Citations (PDF) |
| 202 | Iron- or silver-catalyzed oxidative fluorination of cyclopropanols for the synthesis of β-fluoroketones | 2.6 | 138 | Citations (PDF) |
| 203 | B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>: A New Class of Strong and Bulky Lewis Acid for <i>Exo</i>-Selective Intermolecular Diels–Alder Reactions of Unreactive Acyclic Dienes with α,β-Enals | 4.8 | 63 | Citations (PDF) |
| 204 | Copper- and Cobalt-Catalyzed Direct Coupling of sp<sup>3</sup> α-Carbon of Alcohols with Alkenes and Hydroperoxides | 15.0 | 202 | Citations (PDF) |
| 205 | Rhodium(<scp>iii</scp>)-catalyzed C7-position C–H alkenylation and alkynylation of indolines | 3.4 | 114 | Citations (PDF) |
| 206 | Rhodium(<scp>iii</scp>)-catalyzed C–H allylation of electron-deficient alkenes with allyl acetates | 3.4 | 88 | Citations (PDF) |
| 207 | Rh/Ag Bimetallic Catalyzed C-H Bond Olefination of Benzonitriles | 1.3 | 3 | Citations (PDF) |
| 208 | Asymmetric Conjugate Addition of Grignard Reagents to 3‐Silyl Unsaturated Esters for the Facile Preparation of Enantioenriched β‐Silylcarbonyl Compounds and Allylic Silanes | 3.4 | 25 | Citations (PDF) |
| 209 | Allenamides as Orthogonal Handles for Selective Modification of Cysteine in Peptides and Proteins | 1.4 | 31 | Citations (PDF) |
| 210 | Palladium‐Catalyzed Direct Alkynylation of <i>N</i>‐Vinylacetamides | 3.8 | 69 | Citations (PDF) |
| 211 | Mild Rh(III)-Catalyzed Direct C–H Bond Arylation of (Hetero)Arenes with Arylsilanes in Aqueous Media | 4.8 | 132 | Citations (PDF) |
| 212 | Rhodium‐Catalyzed CH Alkynylation of Arenes at Room Temperature | 14.4 | 226 | Citations (PDF) |
| 213 | Allenamides as Orthogonal Handles for Selective Modification of Cysteine in Peptides and Proteins | 14.4 | 114 | Citations (PDF) |
| 214 | Rhodium(III)-Catalyzed Olefinic C–H Alkynylation of Acrylamides Using Tosyl-Imide as Directing Group | 4.8 | 104 | Citations (PDF) |
| 215 | Palladium-catalyzed amination of allylic carbonates with ammonia: access to primary amines | 4.4 | 7 | Citations (PDF) |
| 216 | Synthesis of multi-substituted vinylsilanes via copper(<scp>i</scp>)-catalyzed hydrosilylation reactions of allenes and propiolate derivatives with silylboronates | 3.4 | 58 | Citations (PDF) |
| 217 | Rhodium(<scp>iii</scp>)-catalyzed olefinic C–H alkynylation of enamides at room temperature | 3.4 | 142 | Citations (PDF) |
| 218 | Preparation of highly substituted (β-acylamino)acrylates via iron-catalyzed alkoxycarbonylation of N-vinylacetamides with carbazates | 3.4 | 60 | Citations (PDF) |
| 219 | Catalytic and direct methyl sulfonylation of alkenes and alkynes using a methyl sulfonyl radical generated from a DMSO, dioxygen and copper system | 7.1 | 184 | Citations (PDF) |
| 220 | Synthesis of multi-substituted pyrroles using enamides and alkynes catalyzed by Pd(OAc)<sub>2</sub>with molecular oxygen as an oxidant | 3.4 | 59 | Citations (PDF) |
| 221 | Iron-Catalyzed Cascade Carbochloromethylation of Activated Alkenes: Highly Efficient Access to Chloro-Containing Oxindoles | 4.8 | 141 | Citations (PDF) |
| 222 | Rhodium(III)-Catalyzed Cross-Coupling of Alkenylboronic Acids and <i>N</i>-Pivaloyloxylamides | 4.8 | 36 | Citations (PDF) |
| 223 | Transition-Metal-Free Synthesis of Substituted Pyridines via Ring Expansion of 2-Allyl-2<i>H-</i>azirines | 4.8 | 110 | Citations (PDF) |
| 224 | Rhodium‐Catalyzed CH Alkynylation of Arenes at Room Temperature | 1.4 | 62 | Citations (PDF) |
| 225 | Directing‐Group‐Assisted Copper‐Catalyzed Olefinic Trifluoromethylation of Electron‐Deficient Alkenes | 14.4 | 152 | Citations (PDF) |
| 226 | Synthesis of Dienyl Ketones via Palladium(II)-Catalyzed Direct Cross-Coupling Reactions between Simple Alkenes and Vinyl Ketones: Application to the Synthesis of Vitamin A1 and Bornelone | 4.8 | 23 | Citations (PDF) |
| 227 | Palladium(ii)-catalyzed cross-coupling of simple alkenes with acrylates: a direct approach to 1,3-dienes through C–H activation | 7.1 | 78 | Citations (PDF) |
| 228 | Diastereoselective oxidative α-amination of aliphatic aldehydes catalyzed by iodine: synthesis of syn-γ-hydroxy-α-amino acetals | 2.6 | 10 | Citations (PDF) |
| 229 | Chemical conversion of β-O-4 lignin linkage models through Cu-catalyzed aerobic amide bond formation | 3.4 | 73 | Citations (PDF) |
| 230 | Organoindium Reagents: The Preparation and Application in Organic Synthesis | 52.7 | 254 | Citations (PDF) |
| 231 | Palladium-catalyzed alkenyl C–H bond sulfonylation reaction using organosulfonyl chlorides | 2.0 | 39 | Citations (PDF) |
| 232 | Pd-catalyzed decarboxylative cross-coupling of perfluorobenzoic acids with simple arenes | 1.4 | 35 | Citations (PDF) |
| 233 | Organocatalytic Synthesis of Highly Functionalized Pyridines at Room Temperature | 14.4 | 81 | Citations (PDF) |
| 234 | Oxidant-Free Rh(III)-Catalyzed Direct C–H Olefination of Arenes with Allyl Acetates | 4.8 | 116 | Citations (PDF) |
| 235 | Radical‐Mediated Diamination of Alkenes with Phenylhydrazine and Azodicarboxylates: Highly Diastereoselective Synthesis of <i>trans</i>‐Diamines from Cycloalkenes | 3.4 | 61 | Citations (PDF) |
| 236 | Asymmetric Hetero-Diels–Alder Reaction of Danishefsky’s Dienes with α-Carbonyl Esters Catalyzed by an Indium(III)–PyBox Complex | 4.8 | 48 | Citations (PDF) |
| 237 | Catalytic Conversion of Inert Carbohydrates into Platform Chemical 5‐Hydroxymethylfurfural Using Arylboronic Acids | 2.3 | 12 | Citations (PDF) |
| 238 | Organocatalytic Synthesis of Highly Functionalized Pyridines at Room Temperature | 1.4 | 18 | Citations (PDF) |
| 239 | Directing‐Group‐Assisted Copper‐Catalyzed Olefinic Trifluoromethylation of Electron‐Deficient Alkenes | 1.4 | 36 | Citations (PDF) |
| 240 | Asymmetric Syntheses of 8‐Oxabicyclo[3,2,1]octanes: A Cationic Cascade Cyclization | 1.4 | 7 | Citations (PDF) |
| 241 | The acid free asymmetric intermolecular α-alkylation of aldehydes in fluorinated alcohols | 3.4 | 79 | Citations (PDF) |
| 242 | α‐Amination of Aldehydes Catalyzed by In Situ Generated Hypoiodite | 1.4 | 25 | Citations (PDF) |
| 243 | Synthesis of 3‐Oxaterpenoids and Its Application in the Total Synthesis of (±)‐Moluccanic Acid Methyl Ester | 1.4 | 21 | Citations (PDF) |
| 244 | Synthesis of 3‐Oxaterpenoids and Its Application in the Total Synthesis of (±)‐Moluccanic Acid Methyl Ester | 14.4 | 42 | Citations (PDF) |
| 245 | Palladium‐Catalyzed Cross‐Coupling of Unactivated Alkenes with Acrylates: Application to the Synthesis of the C13–C21 Fragment of Palmerolide A | 3.4 | 54 | Citations (PDF) |
| 246 | Ruthenium- and rhodium-catalyzed cross-coupling reaction of acrylamides with alkenes: efficient access to (Z,E)-dienamides | 3.4 | 132 | Citations (PDF) |
| 247 | Copper-catalyzed olefinic trifluoromethylation of enamides at room temperature | 7.1 | 264 | Citations (PDF) |
| 248 | Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition | 3.4 | 47 | Citations (PDF) |
| 249 | Application of recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective Diels–Alder reactions | 9.1 | 46 | Citations (PDF) |
| 250 | Palladium‐Catalyzed Direct CH Arylation of Enamides with Simple Arenes | 1.4 | 25 | Citations (PDF) |
| 251 | Catalytic Asymmetric [4+2] Annulation Initiated by an Aza‐Rauhut–Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines | 1.4 | 34 | Citations (PDF) |
| 252 | Palladium‐Catalyzed Direct CH Arylation of Enamides with Simple Arenes | 14.4 | 157 | Citations (PDF) |
| 253 | Asymmetric Syntheses of 8‐Oxabicyclo[3,2,1]octanes: A Cationic Cascade Cyclization | 14.4 | 19 | Citations (PDF) |
| 254 | Catalytic Asymmetric [4+2] Annulation Initiated by an Aza‐Rauhut–Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines | 14.4 | 108 | Citations (PDF) |
| 255 | α‐Amination of Aldehydes Catalyzed by In Situ Generated Hypoiodite | 14.4 | 101 | Citations (PDF) |
| 256 | Rhodium-catalyzed direct ortho C–H olefination of phenol derivatives | 3.4 | 121 | Citations (PDF) |
| 257 | Synthesis and characterization of a cyclic vinylpalladium(ii) complex: vinylpalladium species as the possible intermediate in the catalytic direct olefination reaction of enamide | 7.1 | 151 | Citations (PDF) |
| 258 | Phosphine-catalyzed one-pot isomerization of 3-alkynoates and [2 + 3]-cycloaddition with imines: formal synthesis of Securinega alkaloid (±)-allosecurinine | 7.1 | 87 | Citations (PDF) |
| 259 | In(<scp>iii</scp>)-pybox complex catalyzed enantioselective Mukaiyama aldol reactions between polymeric or hydrated glyoxylates and enolsilanes derived from aryl ketones | 7.1 | 37 | Citations (PDF) |
| 260 | Indium mediated allylation in peptide and protein functionalization | 3.4 | 26 | Citations (PDF) |
| 261 | A New Class of Structurally Rigid Tricyclic Chiral Secondary Amine Organocatalyst: Highly Enantioselective Organocatalytic Michael Addition of Aldehydes to Vinyl Sulfones | 4.8 | 53 | Citations (PDF) |
| 262 | Direct synthesis of ester-containing indium homoenolate and its application in palladium-catalyzed cross-coupling with aryl halide | 3.4 | 43 | Citations (PDF) |
| 263 | Palladium-Catalyzed Cross-Coupling of Indium Homoenolate with Aryl Halide with Wide Functional Group Compatibility | 4.8 | 33 | Citations (PDF) |
| 264 | Copper-catalyzed α-amination of aliphatic aldehydes | 3.4 | 53 | Citations (PDF) |
| 265 | Palladium-Catalyzed C–C Bond Formation of Arylhydrazines with Olefins via Carbon–Nitrogen Bond Cleavage | 4.8 | 111 | Citations (PDF) |
| 266 | Copper-Catalyzed Highly Regioselective Silylcupration of Terminal Alkynes to Form α-Vinylsilanes | 15.0 | 141 | Citations (PDF) |
| 267 | Tripeptide inhibitors of dengue and West Nile virus NS2B–NS3 protease | 3.8 | 91 | Citations (PDF) |
| 268 | A General Strategy for the Introduction of Stereogenic Centers Bearing a Methyl Group: Total Synthesis of Sex Pheromones | 3.0 | 12 | Citations (PDF) |
| 269 | A Facile Synthesis of Highly Substituted Five‐Membered Rings: Mukaiyama‐Aldol‐Oxonoium‐Ene (MAOE) Domino Reaction | 3.0 | 3 | Citations (PDF) |
| 270 | Base‐Free Palladium‐Catalyzed Sonogashira Coupling Using Organogold Complexes | 3.0 | 16 | Citations (PDF) |
| 271 | Highly Enantioselective Intermolecular Alkylation of Aldehydes with Alcohols by Cooperative Catalysis of Diarylprolinol Silyl Ether with Brønsted Acid | 3.0 | 64 | Citations (PDF) |
| 272 | Direct Synthesis of Water‐Tolerant Alkyl Indium Reagents and Their Application in Palladium‐Catalyzed Couplings with Aryl Halides | 1.4 | 8 | Citations (PDF) |
| 273 | Direct Synthesis of Water‐Tolerant Alkyl Indium Reagents and Their Application in Palladium‐Catalyzed Couplings with Aryl Halides | 14.4 | 52 | Citations (PDF) |
| 274 | Indium(III) chloride-catalyzed Mukaiyama–Michael addition: synthesis of 2,6-anti-tetrahydropyrans | 2.0 | 19 | Citations (PDF) |
| 275 | Highly Efficient and Modularly Tuned Bicyclic Organocatalyst for the Enantioselective Michael Addition of Aldehydes to Nitroalkenes | 2.3 | 3 | Citations (PDF) |
| 276 | Hexahydropyrrolo[2,3‐<i>b</i>]indoles: A New Class of Structurally Rigid Tricyclic Skeleton for Oxazaborolidine‐Catalyzed Asymmetric Borane Reduction | 3.8 | 15 | Citations (PDF) |
| 277 | Enantioselective Carbonyl‐Ene Reactions of Trifluoropyruvate in Ionic Liquid <i>via</i> a Recyclable Indium(III)‐Pybox Complex | 3.8 | 36 | Citations (PDF) |
| 278 | Excess Phosphine Ligand Plays a Critical Role in the Asymmetric Copper(I) Iodide‐Catalyzed Conjugate Addition of Grignard Reagents to α,β‐Unsaturated Esters | 3.8 | 14 | Citations (PDF) |
| 279 | Copper‐Catalyzed Rearrangement of Tertiary Amines through Oxidation of Aliphatic CH Bonds in Air or Oxygen: Direct Synthesis of α‐Amino Acetals | 1.4 | 26 | Citations (PDF) |
| 280 | Copper‐Catalyzed Rearrangement of Tertiary Amines through Oxidation of Aliphatic CH Bonds in Air or Oxygen: Direct Synthesis of α‐Amino Acetals | 14.4 | 106 | Citations (PDF) |
| 281 | Highly stereocontrolled synthesis of fluorinated 2,6-trans dihydropyrans via Prins cyclization | 1.4 | 27 | Citations (PDF) |
| 282 | Palladium-catalyzed direct cross-coupling reaction between indenes and electron-deficient alkenes | 1.4 | 43 | Citations (PDF) |
| 283 | Significant counterion effect of the In(III)–pybox complex in highly enantioselective carbonyl-ene reactions of ethyl glyoxylate | 1.4 | 19 | Citations (PDF) |
| 284 | The Organocatalytic Enantioselective Michael Addition of Aldehydes to Vinyl Sulfones in Water | 1.6 | 5 | Citations (PDF) |
| 285 | Highly enantio-, regio- and diastereo-selective one-pot [2 + 3]-cycloaddition reaction via isomerization of 3-butynoates to allenoates, | 7.1 | 131 | Citations (PDF) |
| 286 | Synthesis of Water-Tolerant Indium Homoenolate in Aqueous Media and Its Application in the Synthesis of 1,4-Dicarbonyl Compounds via Palladium-Catalyzed Coupling with Acid Chloride | 15.0 | 111 | Citations (PDF) |
| 287 | Total Synthesis ofPhytophthoraMating Hormone α1 | 4.8 | 21 | Citations (PDF) |
| 288 | Enantioselective Cationic Polyene Cyclization vs Enantioselective Intramolecular Carbonyl−Ene Reaction | 15.0 | 86 | Citations (PDF) |
| 289 | Palladium-Catalyzed Bisolefination of C−C Triple Bonds: A Facile Method for the Synthesis of Naphthalene Derivatives | 15.0 | 98 | Citations (PDF) |
| 290 | Palladium-Catalyzed Oxime Assisted Intramolecular Dioxygenation of Alkenes with 1 atm of Air as the Sole Oxidant | 15.0 | 166 | Citations (PDF) |
| 291 | Chemzymes: A New Class of Structurally Rigid Tricyclic Amphibian Organocatalyst Inspired by Natural Product | 4.8 | 61 | Citations (PDF) |
| 292 | Functionalization of Peptides and Proteins by Mukaiyama Aldol Reaction | 15.0 | 68 | Citations (PDF) |
| 293 | A Facile Method for the Synthesis of Highly Substituted Six-Membered Rings: Mukaiyama−Aldol−Prins Cascade Reaction | 4.8 | 26 | Citations (PDF) |
| 294 | Palladium-catalyzed decarboxylative cross-coupling of alkynyl carboxylic acids with arylboronic acids | 3.4 | 125 | Citations (PDF) |
| 295 | Synthesis of C13-C23 Fragment of Iriomoteolide-1a | 2.3 | 1 | Citations (PDF) |
| 296 | Palladium‐Catalyzed Direct Arylation of Cyclic Enamides with Aryl Silanes by sp<sup>2</sup> CH Activation | 1.4 | 42 | Citations (PDF) |
| 297 | Acid‐Catalyzed Intramolecular [2+2] Cycloaddition of Ene‐allenones: Facile Access to Bicyclo[<i>n</i>.2.0] Frameworks | 1.4 | 11 | Citations (PDF) |
| 298 | Palladium‐Catalyzed Direct Arylation of Cyclic Enamides with Aryl Silanes by sp<sup>2</sup> CH Activation | 14.4 | 200 | Citations (PDF) |
| 299 | Acid‐Catalyzed Intramolecular [2+2] Cycloaddition of Ene‐allenones: Facile Access to Bicyclo[<i>n</i>.2.0] Frameworks | 14.4 | 55 | Citations (PDF) |
| 300 | Indium/copper-mediated conjugate addition of unactivated alkyl iodides to α,β-unsaturated carbonyl compounds in water | 1.4 | 33 | Citations (PDF) |
| 301 | Synthesis of aryl allylic fluorides by direct electrophilic fluorination of alkenes | 1.4 | 27 | Citations (PDF) |
| 302 | An asymmetric synthesis of the polyol fragment of the polyene macrolide antibiotic RK-397 | 1.4 | 24 | Citations (PDF) |
| 303 | One-pot total syntheses of natural products containing a THP-ring backbone: (±)-centrolobine and (±)-civet cat secretion | 1.4 | 34 | Citations (PDF) |
| 304 | Highly Enantioselective Ketone-Ene Reactions of Trifluoropyruvate: Significant Counterion Effect of the In(III)−PyBox Complex | 4.8 | 39 | Citations (PDF) |
| 305 | Intermolecular Hydroamination between Nonactivated Alkenes and Aniline Catalyzed by Lanthanide Salts in Ionic Solvents | 4.8 | 30 | Citations (PDF) |
| 306 | Indium (Zinc)−Copper-Mediated Barbier-Type Alkylation Reaction of Nitrones in Water: Synthesis of Amines and Hydroxylamines | 4.8 | 39 | Citations (PDF) |
| 307 | Direct Cross-Coupling Reaction of Simple Alkenes with Acrylates Catalyzed by Palladium Catalyst | 15.0 | 191 | Citations (PDF) |
| 308 | Synthesis of Iriomoteolide-1a C13−C23 Fragment via Asymmetric Conjugate Addition and Julia−Kocienski Coupling Reaction | 4.8 | 31 | Citations (PDF) |
| 309 | Zn/InCl<sub>3</sub>-Mediated Pinacol Cross-Coupling Reactions of Aldehydes with α,β-Unsaturated Ketones in Aqueous Media | 4.8 | 41 | Citations (PDF) |
| 310 | Design, Synthesis and Optical Resolution of New Bifunctional Ligand: 1,1′-Dimethyl-octahydro-8,8′-Biquinoline-7,7′-diol | 4.8 | 16 | Citations (PDF) |
| 311 | Direct arylation of cyclic enamides via Pd(ii)-catalyzed C–H activation | 3.4 | 101 | Citations (PDF) |
| 312 | Bio-inspired polyene cyclization: aziridinyl polyene cyclization catalyzed by InBr3 | 3.4 | 22 | Citations (PDF) |
| 313 | Silicon as a directing group in the phosphine-catalyzed [2 + 3]-cycloaddition of aryl allenones with electron-deficient olefins | 3.4 | 76 | Citations (PDF) |
| 314 | Stereoelectronic versus Steric Tuning in the Prins Cyclization Reaction: Synthesis of 2,6-<i>trans</i> Pyranyl Motifs | 4.8 | 48 | Citations (PDF) |
| 315 | Enantioselective direct vinylogous Michael addition reaction catalyzed by organic molecules | 1.4 | 27 | Citations (PDF) |
| 316 | Enantioselective epoxidation of α,β-enones promoted by (1R,3S,4S)-2-azanorbornyl-3-methanol as an organocatalyst | 1.4 | 47 | Citations (PDF) |
| 317 | Unexpected domino ring closure: highly stereoselective construction of a tetracyclic indole alkaloid ring system | 1.4 | 14 | Citations (PDF) |
| 318 | Indium–Silver‐ and Zinc–Silver‐Mediated Barbier–Grignard‐Type Alkylation Reactions of Imines by Using Unactivated Alkyl Halides in Aqueous Media | 3.4 | 49 | Citations (PDF) |
| 319 | An In‐Mediated Tandem Reaction of Aldehydes with 3‐Bromo‐1‐propyne To Produce 1‐Substituted‐3‐methylene‐5‐yn‐1‐ol Compounds | 2.3 | 13 | Citations (PDF) |
| 320 | Highly Efficient Copper(I) Iodide‐Tolyl‐BINAP‐Catalyzed Asymmetric Conjugate Addition of Methylmagnesium Bromide to α,β‐Unsaturated Esters | 3.8 | 40 | Citations (PDF) |
| 321 | Enantioselective Michael Addition of Dicyanoolefins to α,β‐Unsaturated Aldehydes in Aqueous Medium | 3.8 | 58 | Citations (PDF) |
| 322 | Organocatalytic and Enantioselective Direct Vinylogous Michael Addition to Maleimides | 3.8 | 75 | Citations (PDF) |
| 323 | Practical synthesis of 1,5-dimethyl substituted conjugated polyenes from geranyl acetate | 2.0 | 11 | Citations (PDF) |
| 324 | Indium(III) iodide-mediated Strecker reaction in water: an efficient and environmentally friendly approach for the synthesis of α-aminonitrile via a three-component condensation | 2.0 | 85 | Citations (PDF) |
| 325 | Asymmetric Total Synthesis of Antiochic Acid | 4.8 | 26 | Citations (PDF) |
| 326 | A Simple Approach To Separate a Mixture of Homopropargylic and Allenic Alcohols | 4.8 | 15 | Citations (PDF) |
| 327 | Highly Enantioselective Carbonyl-ene Reactions Catalyzed by In(III)−PyBox Complex | 15.0 | 74 | Citations (PDF) |
| 328 | Control of up to Five Stereocenters in a Cascade Reaction: Synthesis of Highly Functionalized Five-Membered Rings | 15.0 | 41 | Citations (PDF) |
| 329 | Bio-inspired polyene cyclization: synthesis of tetracyclic terpenoids promoted by steroidal acetal–SnCl4 | 3.4 | 12 | Citations (PDF) |
| 330 | Indium tribromide-promoted arene-terminated epoxy olefin cyclization | 3.4 | 42 | Citations (PDF) |
| 331 | One-pot chemoenzymatic syntheses of enantiomerically-enriched O-acetyl cyanohydrins from aldehydes in ionic liquid | 9.1 | 41 | Citations (PDF) |
| 332 | Homoallyllic Nitrone Isomerization: Convenient Enantioselective Synthesis of Homoallylic Nitrones and Homoallylic Hydroxylamines | 4.8 | 17 | Citations (PDF) |
| 333 | Bioinspired Polyene Cyclization Promoted by Intermolecular Chiral Acetal-SnCl<sub>4</sub>or Chiral<i>N</i>-Acetal-TiCl<sub>4</sub>: Investigation of the Mechanism and Identification of the Key Intermediates | 15.0 | 51 | Citations (PDF) |
| 334 | A Highly Catalytic Asymmetric Conjugate Addition: Synthesis of the C14−C20 Fragment of Antibiotic TMC-151A, Siphonarienal and Siphonarienone | 4.8 | 48 | Citations (PDF) |
| 335 | Highly Stereoselective Prins Cyclization of (Z)- and (E)-γ-Brominated Homoallylic Alcohols to 2,4,5,6-Tetrasubstituted Tetrahydropyrans | 4.8 | 77 | Citations (PDF) |
| 336 | Lewis Acid-Promoted Intermolecular Acetal-Initiated Cationic Polyene Cyclizations | 15.0 | 75 | Citations (PDF) |
| 337 | Formal synthesis of (+)-SCH 351448: the Prins cyclization approach | 3.4 | 61 | Citations (PDF) |
| 338 | Stannane-Free Chemoselective Hydrodehalogenation of 4-Halotetrahydropyrans: Scope and Application to Natural Product Synthesis | 3.5 | 6 | Citations (PDF) |
| 339 | Indium−Copper-Mediated Barbier−Grignard-Type Alkylation Reaction of Imines in Aqueous Media | 4.8 | 58 | Citations (PDF) |
| 340 | Cu(I) Tol-BINAP-Catalyzed Enantioselective Michael Reactions of Grignard Reagents and Unsaturated Esters | 15.0 | 128 | Citations (PDF) |
| 341 | Stereochemical Prins cyclization: electronic versus steric effects on the synthesis of 2,4,6-trisubstituted tetrahydropyran rings | 1.4 | 34 | Citations (PDF) |
| 342 | Diastereoselective allylation of planar chiral substituted ferrocenecarboxaldehyde: an efficient entry to chiral ferrocenyl ligands | 1.4 | 14 | Citations (PDF) |
| 343 | InBr3 Catalyzed intermolecular hydroamination of unactivated alkenes | 1.4 | 50 | Citations (PDF) |
| 344 | Microwave-assisted synthesis of photochromic fulgimides | 4.3 | 8 | Citations (PDF) |
| 345 | Total synthesis of antillatoxin | 3.4 | 25 | Citations (PDF) |
| 346 | Catalytic Enantioselective Diels−Alder Reaction in Ionic Liquid via a Recyclable Chiral In(III) Complex | 4.8 | 52 | Citations (PDF) |
| 347 | A highly enantioselective one-pot synthesis of homoallylic alcohols via tandem asymmetric allyl transfer/olefin cross metathesis | 1.4 | 20 | Citations (PDF) |
| 348 | Suppression of epimerization due to selectivity leakage: an application towards the total synthesis of (−)-centrolobine | 1.4 | 58 | Citations (PDF) |
| 349 | Catalytic enantioselective Mukaiyama aldol reaction via a chiral indium(III)–pybox complex | 1.4 | 32 | Citations (PDF) |
| 350 | Synthetic studies toward the total synthesis of tedanolide: assembly of the C1–C23 carbon backbone | 1.4 | 18 | Citations (PDF) |
| 351 | General and practical approach to the syntheses of linear homoallylic alcohols | 2.0 | 9 | Citations (PDF) |
| 352 | Activation of Reactions by Lewis Acids Derived from Ga, In, Sb and Bi | 0.4 | 7 | Citations (PDF) |
| 353 | Ionic liquid [omim][PF6] as an efficient and recyclable reaction media for the cyanosilylation of aldehydes without Lewis acid or any special activation | 1.4 | 41 | Citations (PDF) |
| 354 | Catalytic enantioselective allylation of aldehydes via a chiral indium(III) complex in ionic liquids | 1.4 | 18 | Citations (PDF) |
| 355 | Catalytic enantioselective allylation of aldehydes via a moisture-tolerant chiral BINOL–In(III) complex | 1.4 | 25 | Citations (PDF) |
| 356 | Asymmetric allyltributylstannane addition to ketones catalyzed by chiral PYBOX–In(III) complex immobilized in ionic liquid | 1.4 | 37 | Citations (PDF) |
| 357 | An environmentally friendly procedure for Mukaiyama aldol and Mukaiyama–Michael reactions using a catalytic amount of DBU under solvent- and metal-free conditions | 1.4 | 46 | Citations (PDF) |
| 358 | Catalytic Enantioselective Allylation of Ketones via a Chiral Indium(III) Complex | 4.8 | 93 | Citations (PDF) |
| 359 | Catalytic Enantioselective Diels−Alder Reaction via a Chiral Indium(III) Complex | 4.8 | 55 | Citations (PDF) |
| 360 | Enantioselective allylation of ketones catalyzed by chiral In(iii)-PYBOX complexes | 3.4 | 57 | Citations (PDF) |
| 361 | Enantioselective synthesis of homoallylic alcohols via a chiral In(iii)–PYBOX complex | 3.4 | 37 | Citations (PDF) |
| 362 | Catalytic asymmetric allylation of aldehydes via a chiral indium(iii) complex | 3.4 | 57 | Citations (PDF) |
| 363 | Highly Enantioselective Allylation of Aldehydes Catalyzed by Indium(III)−PYBOX Complex | 4.8 | 86 | Citations (PDF) |
| 364 | Gram-Scale Synthesis of (−)-Epibatidine | 4.8 | 44 | Citations (PDF) |
| 365 | Prins Cyclizations in Silyl Additives with Suppression of Epimerization: Versatile Tool in the Synthesis of the Tetrahydropyran Backbone of Natural Products | 4.8 | 128 | Citations (PDF) |
| 366 | Enantioselective allylation of aldehydes catalyzed by chiral indium(iii) complexes immobilized in ionic liquids | 3.4 | 40 | Citations (PDF) |
| 367 | Efficient FeIII-Catalyzed Synthesis of Bis(indolyl)methanes in Ionic Liquids | 2.3 | 160 | Citations (PDF) |
| 368 | Mukaiyama aldol reaction using ketene silyl acetals with carbonyl compounds in ionic liquids | 1.4 | 30 | Citations (PDF) |
| 369 | A highly enantioselective allyl-transfer through suppression of epimerization | 1.4 | 21 | Citations (PDF) |
| 370 | Lewis acid-catalyzed one-pot crossed Prins cyclizations using allylchlorosilane as allylating agent | 1.4 | 57 | Citations (PDF) |
| 371 | Synthetic studies towards anti-SARS agents: application of an indium-mediated allylation of α-aminoaldehydes as the key step towards an intermediate | 1.4 | 12 | Citations (PDF) |
| 372 | Facile synthesis of bis(indolyl)methanes using catalytic amount of iodine at room temperature under solvent-free conditions | 2.0 | 248 | Citations (PDF) |
| 373 | Silicon-assisted propargylic transfer to aldehydes | 3.4 | 36 | Citations (PDF) |
| 374 | An Unusual Approach to the Synthesis of Enantiomerically Cis Linear Homoallylic Alcohols Based on the Steric Interaction Mechanism of Camphor Scaffold | 4.8 | 64 | Citations (PDF) |
| 375 | Highly Efficient Chemical Kinetic Resolution of Bishomoallylic Alcohols: Synthesis of (R)-Sulcatol | 4.8 | 20 | Citations (PDF) |
| 376 | Indium-mediated propargylation of aldehydes: regioselectivity and enantioselectivity studies | 1.4 | 61 | Citations (PDF) |
| 377 | Indium-mediated allylation of carbonyl compounds with an allylic bromide in aqueous media: anomalous syn-diastereoselectivity regardless of allylic bromide geometry | 1.4 | 35 | Citations (PDF) |
| 378 | Asymmetric Mannich-type reactions catalyzed by indium(III) complexes in ionic liquids | 1.4 | 47 | Citations (PDF) |
| 379 | A divergent approach to apoptolidin and FD-891: asymmetric preparation of a common intermediate | 1.4 | 23 | Citations (PDF) |
| 380 | Indium-Mediated Reaction of Trialkylsilyl Propargyl Bromide with Aldehydes: Highly Regioselective Synthesis of Allenic and Homopropargylic Alcohols | 15.0 | 104 | Citations (PDF) |
| 381 | A Novel and General α-Regioselective and Highly Enantioselective Prenylation of Aldehydes | 15.0 | 34 | Citations (PDF) |
| 382 | Development of a Highly α-Regioselective Metal-Mediated Allylation Reaction in Aqueous Media: New Mechanistic Proposal for the Origin of α-Homoallylic Alcohols | 15.0 | 151 | Citations (PDF) |
| 383 | Indium-Mediated Allylation Reaction in Aqueous Media: Synthetic Studies Towards the Total Synthesis of Dysiherbaine | 2.3 | 5 | Citations (PDF) |
| 384 | Indium(III) Complex-Catalyzed Tandem Carbonyl-Ene Reaction: An Efficient Construction of Tetrahydropyran Rings | 2.3 | 20 | Citations (PDF) |
| 385 | The First Example of Enantioselective Allyl Transfer from a Linear Homoallylic Alcohol to an Aldehyde | 4.8 | 35 | Citations (PDF) |
| 386 | Stereocontrolled Synthesis of Linear 22R-Homoallylic Sterols via a Triflic Acid-Catalyzed 2-Oxonia Cope Rearrangement | 4.8 | 25 | Citations (PDF) |
| 387 | Nickel-Catalyzed Homoallylation Reaction of Aldehydes with 1,3-Dienes: Stereochemical and Mechanistic Studies | 4.8 | 44 | Citations (PDF) |
| 388 | InCl3-Catalyzed Three-Component Asymmetric Mannich-Type Reaction in Methanol | 4.8 | 88 | Citations (PDF) |
| 389 | Diastereoselective construction of cis 2,6-disubstituted tetrahydropyran rings via In(OTf)3-catalyzed intramolecular 2,5-oxonium-ene cyclization: synthetic studies towards the total synthesis of zampanolide and dactylolide | 1.4 | 35 | Citations (PDF) |
| 390 | l-Proline in an ionic liquid as an efficient and reusable catalyst for direct asymmetric aldol reactions | 1.4 | 169 | Citations (PDF) |
| 391 | Diverse Cyclization Catalyzed by In(OTf)3 for the Convergent Assembly of Substituted Tetrahydrofurans and Tetrahydropyrans | 4.8 | 93 | Citations (PDF) |
| 392 | Formation of Tetrahydrofuran from Homoallylic Alcohol via a Tandem Sequence: 2-Oxonia [3,3]-Sigmatropic Rearrangement/Cyclization Catalyzed by In(OTf)3 | 15.0 | 94 | Citations (PDF) |
| 393 | Synthetic studies toward kaitocephalin | 1.4 | 10 | Citations (PDF) |
| 394 | Development of a highly α-regioselective indium-mediated allylation reaction in water | 1.4 | 39 | Citations (PDF) |
| 395 | A new mechanistic proposal for the origin of α-homoallylic alcohols in indium-mediated allylation reactions in water | 1.4 | 36 | Citations (PDF) |
| 396 | Homoallylic sterol/indium(III) Lewis acid: a novel enantioselective allylation system exhibiting α-regioselectivity | 1.4 | 28 | Citations (PDF) |
| 397 | InCl3-Catalyzed direct aldol reactions of glyoxylic acid monohydrate and glyoxylates with various ketones: scope and limitations | 2.0 | 14 | Citations (PDF) |
| 398 | Synthetic studies towards the total synthesis of tedanolide: formation of the C(13)–C(23) fragment | 1.4 | 45 | Citations (PDF) |
| 399 | A concise synthesis of (±)-methylenolactocin and the formal synthesis of (±)-phaseolinic acid | 1.4 | 36 | Citations (PDF) |
| 400 | Progress towards the total synthesis of tedanolide: an efficient assembly of the C1–C11 subunit | 1.4 | 29 | Citations (PDF) |
| 401 | The First In(OTf)3-Catalyzed Conversion of Kinetically Formed Homoallylic Alcohols into the Thermodynamically Preferred Regioisomers: Application to the Synthesis of 22α-Sterols | 1.4 | 8 | Citations (PDF) |
| 402 | The First In(OTf)3-Catalyzed Conversion of Kinetically Formed Homoallylic Alcohols into the Thermodynamically Preferred Regioisomers: Application to the Synthesis of 22α-Sterols | 14.4 | 51 | Citations (PDF) |
| 403 | Synthetic Studies toward Anisatin: A Formal Synthesis of (±)-8-Deoxyanisatin | 4.8 | 46 | Citations (PDF) |
| 404 | Water-Accelerated Aldol Reaction of Ketene Silyl Acetals with Carbonyl Compounds | 2.0 | 48 | Citations (PDF) |
| 405 | A remote substituent as a control element in indium-mediated allylation reactions in aqueous media: highly diastereoselective synthesis of 1,3-amino alcohols | 1.4 | 31 | Citations (PDF) |
| 406 | A highly regioselective indium-mediated allylation of pyridine derivatives: synthesis of (±)-dihydropinidine from pyridine | 1.4 | 35 | Citations (PDF) |
| 407 | A highly chemoselective and diastereoselective trifluoromethane sulfonic acid catalyzed addition of allyltributylstannanes to a steroidal aldehyde in aqueous media | 1.6 | 19 | Citations (PDF) |
| 408 | Three Component Synthesis of β-Amino Carbonyl Compounds Using Indium Trichloride-Catalyzed One-pot Mannich-type Reaction in Water | 2.0 | 125 | Citations (PDF) |
| 409 | A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium | 1.4 | 62 | Citations (PDF) |
| 410 | Aldol Reaction under Solvent-Free Conditions: Highly Stereoselective Synthesis of 1,3-Amino Alcohols | 4.8 | 64 | Citations (PDF) |
| 411 | Trifluoromethane sulphonic acid: a Brönsted acid catalyst for the addition of allyltributylstannanes to carbonyl compounds in water | 1.4 | 41 | Citations (PDF) |
| 412 | A new method for the synthesis of β,γ-unsaturated amides from allylic carbonate catalyzed by palladium in the presence of carbon monoxide and amine: Studies towards the total synthesis of antillatoxin | 1.4 | 17 | Citations (PDF) |
| 413 | A novel reductive aminocyclization for the syntheses of chiral pyrrolidines: stereoselective syntheses of (S)-nornicotine and 2-(2′-pyrrolidyl)-pyridines | 1.4 | 16 | Citations (PDF) |
| 414 | An enantioselective allylation reaction of aldehydes in an aqueous medium | 1.4 | 66 | Citations (PDF) |
| 415 | Competitive fine-tuning of heteroaromatic imines as dienophiles or dienes in the Lewis acid-mediated Diels-Alder reaction with cyclopentadiene | 1.4 | 12 | Citations (PDF) |
| 416 | An enantioselective indium-mediated allylation reaction of aldehydes and ketones in dichloromethane | 1.4 | 66 | Citations (PDF) |
| 417 | A simple and practical synthesis of α-trifluoromethylated alcohols in water | 2.0 | 30 | Citations (PDF) |
| 418 | Clay montmorillonite K10 catalyzed aldol-type reaction of aldehydes with silyl enol ethers in water | 2.0 | 39 | Citations (PDF) |
| 419 | Tin- and Indium-Mediated Allylation Reactions in Water: Highly Stereoselective Synthesis of β-Trifluoromethylated Homoallylic Alcohols | 2.3 | 36 | Citations (PDF) |
| 420 | A Highly Enantioselective Indium-Mediated Allylation Reaction of Aldehydes | 4.8 | 103 | Citations (PDF) |
| 421 | Novel one-pot Mannich-type reaction in water: Indium trichloride-catalyzed condensation of aldehydes, amines and silyl enol ethers for the synthesis of β-amino ketones and esters | 1.4 | 128 | Citations (PDF) |
| 422 | Indium-trichloride catalyzed Michael reaction of silyl enol ethers with α,β-unsaturated carbonyl compounds under neat condition | 2.0 | 45 | Citations (PDF) |
| 423 | Studies towards total synthesis of antillatoxin: Investigation of the indium-mediated allylation reactions of carbonyl compounds with β-bromocrotylbromide in water | 1.4 | 52 | Citations (PDF) |
| 424 | Studies towards total synthesis of antillatoxin: Synthesis of C1C11 fragment | 1.4 | 32 | Citations (PDF) |
| 425 | Highly stereoselective indium trichloride-catalysed asymmetric aldol reaction of formaldehyde and a glucose-derived silyl enol ether in water | 3.4 | 36 | Citations (PDF) |
| 426 | LANTHANOID TRIFLATE-PROMOTED INDIUM- OR ZINC-MEDIATED ALLYLATION OF AMINOALDEHYDE IN AQUEOUS MEDIA: STEREOSELECTIVE ROUTE TO ß-AMINOALCOHOLS | 1.1 | 11 | Citations (PDF) |
| 427 | Synthesis of Heterocyclic Analogues of Tamoxifen asPotential Antiestrogens | 0.4 | 6 | Citations (PDF) |
| 428 | A highly stereoselective one-pot asymmetric synthesis of homoallylic amines and amino acids from aldehydes | 1.4 | 69 | Citations (PDF) |
| 429 | A novel method for stereoselective synthesis of β-trifluoromethylated homoallylic alcohols in water | 1.4 | 38 | Citations (PDF) |
| 430 | Indium-trichloride catalyzed mukaiyama-aldol reaction in water: Solubility, aggregation and internal pressure effect | 1.4 | 43 | Citations (PDF) |
| 431 | A Highly Stereoselective Synthesis ofβ-Trifluoromethylated Homoallylic Alchols in Water | 4.7 | 68 | Citations (PDF) |
| 432 | Hochstereoselektive Synthese von β‐trifluormethylierten Homoallylalkoholen in Wasser | 1.4 | 11 | Citations (PDF) |
| 433 | A versatile and practical synthesis of α-trifluoromethylated alcohols from trifluoroacetaldehyde ethyl hemiacetal in water | 3.4 | 39 | Citations (PDF) |
| 434 | Indium trichloride (InCl3) catalysed Diels–Alder reaction in water | 3.4 | 118 | Citations (PDF) |
| 435 | Indium trichloride catalysed Mukaiyama aldol reaction in water | 3.4 | 87 | Citations (PDF) |
| 436 | Chiral tartrate-derived dioxaborolidine: A simple and practical catalyst for enantioselective Diels-Alder reaction | 1.4 | 17 | Citations (PDF) |
| 437 | Indium trichloride-promoted tin-mediated carbonyl allylation in water: High simple diastereo- and diastereofacial selectivity | 1.6 | 95 | Citations (PDF) |
| 438 | Ytterbium trifluoromethanesulfonate [Yb(OTf)3] promoted indium mediated allylation reactions of carbonyl compounds in aqueous media | 1.6 | 54 | Citations (PDF) |
| 439 | Demonstration of the Synthetic Power of Oxazaborolidine-Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberellic Acid | 15.0 | 104 | Citations (PDF) |
| 440 | A unified approach to (22S)- or (22R)-hydroxy steroid side chain: Lewis acid-promoted carbonyl-ene reaction with α-alkoxyaldehydes | 1.9 | 5 | Citations (PDF) |
| 441 | Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products | 1.4 | 150 | Citations (PDF) |
| 442 | Stereocontrolled total synthesis of (+)- and (-)-epibatidine | 3.5 | 99 | Citations (PDF) |
| 443 | The origin of greater than 200:1 enantioselectivity in a catalytic Diels-Alder reaction as revealed by physical and chemical studies | 15.0 | 171 | Citations (PDF) |
| 444 | The structure of the 2-methylacrolein boron trifluoride complex in the crystalline phase and in solution | 1.4 | 50 | Citations (PDF) |
| 445 | Acyclic stereocontrol based on nonchelation-controlled ene reactions with α-haloaldehydes | 1.9 | 9 | Citations (PDF) |
| 446 | First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions | 15.0 | 270 | Citations (PDF) |
| 447 | Acyclic stereocontrol based on chelation-controlled ene reaction with chiral α- and β-alkoxyaldehydes | 1.6 | 39 | Citations (PDF) |
| 448 | Carbonyl-ene reaction with vinylsilanes: silicon as a controlling element for regio- and stereochemistry | 15.0 | 31 | Citations (PDF) |
| 449 | Anomalous threo-diastereoselectivity in allylic silane- or stannane–aldehyde condensation reactions: new interpretation of the antiperiplanar vs. synclinal problem on the transition-state conformations | 1.9 | 35 | Citations (PDF) |
| 450 | Diastereocontrol via lewis acid-promoted ene reaction with glyoxylates and its application to stereocontrolled synthesis of a 22-hydroxy-23-carboxylate steroid side chain | 1.4 | 48 | Citations (PDF) |
| 451 | Ene approach for concurrent control over the chiral centres at C-20 and C-22 of steroid side chains: a highly stereocontrolled synthesis of (20S,22R)-(erythro-)22-hydroxy-23,24-acetylenic steroid side chains | 1.9 | 16 | Citations (PDF) |
| 452 | Thiol‐Specific Silicon‐Containing Conjugating Reagent: <i>β</i>‐Silyl Alkynyl Carbonyl Compounds | 1.4 | 0 | Citations (PDF) |
