| 1 | [4+1] Heteroannulation to Form 1‐Pyrrolines through Alder‐Ene Reaction of in situ Generated Ynimines: Development and Application in Total Synthesis of Borrecapine | 14.4 | 9 | Citations (PDF) |
| 2 | [4+1] Heteroannulation to Form 1‐Pyrrolines through Alder‐Ene Reaction of in situ Generated Ynimines: Development and Application in Total Synthesis of Borrecapine | 1.4 | 1 | Citations (PDF) |
| 3 | Chemoselectivity in Pd-Based Dyotropic Rearrangement: Development and Application in Total Synthesis of Pheromones | 15.0 | 10 | Citations (PDF) |
| 4 | Asymmetric Synthesis of Inherently Chiral Tetraoxacalix[2]arene[2]pyridines via SNAr‐Based Cross‐Cyclotetramerization | 3.0 | 4 | Citations (PDF) |
| 5 | Total Synthesis of Discobahamin A and Putative Structure of Discobahamin B via an Isocyanide‐based Macrocyclization Reaction | 14.4 | 0 | Citations (PDF) |
| 6 | Total Synthesis of Discobahamin A and Putative Structure of Discobahamin B via an Isocyanide‐based Macrocyclization Reaction | 1.4 | 0 | Citations (PDF) |
| 7 | Pd-Catalyzed Strain-Releasing Dyotropic Rearrangement: Ring-Expanding Amidofluorination of Methylenecyclobutanes | 15.0 | 7 | Citations (PDF) |
| 8 | Divergent Enantioselective Total Synthesis of (−)-Ajmalicine, (+)-Mayumbine, and (−)-Roxburghine C | 4.8 | 5 | Citations (PDF) |
| 9 | C4-Symmetric Inherently Chiral Macrocycles from Organocatalytic Enantioselective Desymmetrization of Resorcin[4]arenes | 12.4 | 6 | Citations (PDF) |
| 10 | Chiral Phosphoric Acid-Catalyzed Enantioselective Higher-Order Cycloadditions: Temperature-Dependent Periselectivity | 15.0 | 2 | Citations (PDF) |
| 11 | Palladium‐Based Dyotropic Rearrangement Enables A Triple Functionalization of Gem‐Disubstituted Alkenes: An Unusual Fluorolactonization Reaction | 14.4 | 19 | Citations (PDF) |
| 12 | Palladium‐Based Dyotropic Rearrangement Enables A Triple Functionalization of Gem‐Disubstituted Alkenes: An Unusual Fluorolactonization Reaction | 1.4 | 3 | Citations (PDF) |
| 13 | Chalcogen bonding catalysis | 37.7 | 84 | Citations (PDF) |
| 14 | Benzylic C(sp3)−H Azidation: Copper vs Iron Catalysis | 1.8 | 5 | Citations (PDF) |
| 15 | Arylative Ring Expansion of 3‐Vinylazetidin‐3‐Ols and 3‐Vinyloxetan‐3‐Ols to Dihydrofurans by Dual Palladium and Acid Catalysis | 1.4 | 0 | Citations (PDF) |
| 16 | Arylative Ring Expansion of 3‐Vinylazetidin‐3‐Ols and 3‐Vinyloxetan‐3‐Ols to Dihydrofurans by Dual Palladium and Acid Catalysis | 14.4 | 4 | Citations (PDF) |
| 17 | Catalytic Enantioselective Synthesis of Inherently Chiral Macrocycles by Dynamic Kinetic Resolution | 12.4 | 24 | Citations (PDF) |
| 18 | Inherently chiral nor-heteracalixarenes: design and synthesis
via
enantioselective intramolecular Suzuki–Miyaura reaction | 7.1 | 19 | Citations (PDF) |
| 19 | Quaternary Carbon Editing Enabled by Sequential Palladium Migration | 15.0 | 12 | Citations (PDF) |
| 20 | Chemoselective Pd-Based Dyotropic Rearrangement: Fluorocyclization and Regioselective Wacker Reaction of Homoallylic Amides | 15.0 | 13 | Citations (PDF) |
| 21 | Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A | 1.4 | 4 | Citations (PDF) |
| 22 | Organocatalytic Enantioselective Diels–Alder Reaction of 2‐Trifluoroacetamido‐1,3‐dienes with α,β‐Unsaturated Ketones | 14.4 | 19 | Citations (PDF) |
| 23 | Organocatalytic Enantioselective Diels–Alder Reaction of 2‐Trifluoroacetamido‐1,3‐dienes with α,β‐Unsaturated Ketones | 1.4 | 2 | Citations (PDF) |
| 24 | Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A | 14.4 | 33 | Citations (PDF) |
| 25 | Inherently chiral calixarenes by a catalytic enantioselective desymmetrizing cross-dehydrogenative coupling | 7.1 | 80 | Citations (PDF) |
| 26 | Highly Strained Oxygen‐Doped Chiral Molecular Belts of the Zigzag‐Type with Strong Circularly Polarized Luminescence | 14.4 | 30 | Citations (PDF) |
| 27 | Highly Strained Oxygen‐Doped Chiral Molecular Belts of the Zigzag‐Type with Strong Circularly Polarized Luminescence | 1.4 | 0 | Citations (PDF) |
| 28 | Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B | 14.4 | 10 | Citations (PDF) |
| 29 | Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B | 1.4 | 2 | Citations (PDF) |
| 30 | Enantioselective Total Synthesis of (+)-Stephadiamine | 15.0 | 17 | Citations (PDF) |
| 31 | Asymmetric Construction of α,α‐Disubstituted Piperazinones Enabled by Benzilic Amide Rearrangement | 14.4 | 27 | Citations (PDF) |
| 32 | Asymmetric Construction of α,α‐Disubstituted Piperazinones Enabled by Benzilic Amide Rearrangement | 1.4 | 1 | Citations (PDF) |
| 33 | Terminal Alkynes as One‐Carbon Donors in [5+1] Heteroannulation: Synthesis of Pyridines via Ynimine Intermediates and Application in the Total Synthesis of Anibamine B | 1.4 | 2 | Citations (PDF) |
| 34 | Oxidative rearrangement of 1,1-disubstituted alkenes to ketones | 36.2 | 51 | Citations (PDF) |
| 35 | Dual Photoredox and Copper Catalysis: Enantioselective 1,2-Amidocyanation of 1,3-Dienes | 12.4 | 38 | Citations (PDF) |
| 36 | Terminal Alkynes as One‐Carbon Donors in [5+1] Heteroannulation: Synthesis of Pyridines via Ynimine Intermediates and Application in the Total Synthesis of Anibamine B | 14.4 | 12 | Citations (PDF) |
| 37 | Asymmetric Synthesis of Enantioenriched Zigzag-Type Molecular Belts by Kinetic Resolution and Subsequent Transformations | 4.8 | 20 | Citations (PDF) |
| 38 | Diverting the 5-exo-Trig Oxypalladation to Formally 6-endo-Trig Fluorocycloetherification Product through 1,2-O/Pd(IV) Dyotropic Rearrangement | 15.0 | 23 | Citations (PDF) |
| 39 | Enantioselective Total Synthesis of (−)-Artatrovirenol A | 15.0 | 23 | Citations (PDF) |
| 40 | Two-Carbon Ring Expansion of Cyclobutanols to Cyclohexenones Enabled by Indole Radical Cation Intermediate: Development and Application to a Total Synthesis of Uleine | 12.4 | 25 | Citations (PDF) |
| 41 | Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst | 14.4 | 37 | Citations (PDF) |
| 42 | Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst | 1.4 | 6 | Citations (PDF) |
| 43 | Modular Synthesis of Benzocyclobutenes via Pd(II)-Catalyzed Oxidative [2+2] Annulation of Arylboronic Acids with Alkenes | 15.0 | 26 | Citations (PDF) |
| 44 | Taming the radical cation intermediate enabled one-step access to structurally diverse lignans | 13.7 | 15 | Citations (PDF) |
| 45 | Migrative Carbofluorination of Saturated Amides Enabled by Pd-Based Dyotropic Rearrangement | 15.0 | 31 | Citations (PDF) |
| 46 | Thiazole Boron Difluoride Dyes with Large Stokes Shift, Solid State Emission and Room‐Temperature Phosphorescence | 3.4 | 4 | Citations (PDF) |
| 47 | Synthesis of 3-Acyloxyindolenines by TiCl3-Mediated Reductive Cyclization of 2-(ortho-Nitroaryl)-Substituted Enol Esters | 4.8 | 7 | Citations (PDF) |
| 48 | Apparent 6‐endo‐trig Carbofluorination of Alkenes Enabled by Palladium‐Based Dyotropic Rearrangement | 14.4 | 29 | Citations (PDF) |
| 49 | Apparent 6‐endo‐trig Carbofluorination of Alkenes Enabled by Palladium‐Based Dyotropic Rearrangement | 1.4 | 1 | Citations (PDF) |
| 50 | Selective 1,2‐Aminoisothiocyanation of 1,3‐Dienes Under Visible‐Light Photoredox Catalysis | 14.4 | 108 | Citations (PDF) |
| 51 | Selective 1,2‐Aminoisothiocyanation of 1,3‐Dienes Under Visible‐Light Photoredox Catalysis | 1.4 | 2 | Citations (PDF) |
| 52 | Unified divergent strategy towards the total synthesis of the three sub-classes of hasubanan alkaloids | 13.7 | 26 | Citations (PDF) |
| 53 | Catalytic Enantioselective Aminopalladation–Heck Cascade | 14.4 | 54 | Citations (PDF) |
| 54 | Catalytic Enantioselective Aminopalladation–Heck Cascade | 1.4 | 3 | Citations (PDF) |
| 55 | Enantioselective Total Synthesis of (+)‐Alstilobanine C, (+)‐Undulifoline, and (−)‐Alpneumine H | 1.4 | 0 | Citations (PDF) |
| 56 | Enantioselective Total Synthesis of (+)‐Alstilobanine C, (+)‐Undulifoline, and (−)‐Alpneumine H | 14.4 | 15 | Citations (PDF) |
| 57 | Natural Product Synthesis Enabled by Domino Processes Incorporating a 1,2-Rearrangement Step | 9.2 | 78 | Citations (PDF) |
| 58 | Catalytic Enantioselective Synthesis of Morpholinones Enabled by Aza-Benzilic Ester Rearrangement | 15.0 | 39 | Citations (PDF) |
| 59 | C–C bond activation enabled by dyotropic rearrangement of Pd(iv) species | 18.8 | 72 | Citations (PDF) |
| 60 | Enantioselective Total Synthesis of (+)‐Nordasycarpidone, (+)‐Dasycarpidone, and (+)‐Uleine | 1.8 | 7 | Citations (PDF) |
| 61 | Photoredox Catalytic Three-Component Amidoazidation of 1,3-Dienes | 12.4 | 71 | Citations (PDF) |
| 62 | Copper‐Catalyzed Aza‐Sonogashira Cross‐Coupling To Form Ynimines: Development and Application to the Synthesis of Heterocycles | 14.4 | 33 | Citations (PDF) |
| 63 | Visible light photoredox-catalysed remote C–H functionalisation enabled by 1,5-hydrogen atom transfer (1,5-HAT) | 37.7 | 371 | Citations (PDF) |
| 64 | Fused N‐Heterocycles with Contiguous Stereogenic Centers Accessed by an Asymmetric Catalytic Cascade Reaction of Tertiary Enamides | 3.4 | 18 | Citations (PDF) |
| 65 | Organocatalytic Double Ugi Reaction with Statistical Amplification of Product Enantiopurity: A Linker Cleavage Approach To Access Highly Enantiopure Ugi Products | 4.8 | 20 | Citations (PDF) |
| 66 | Desymmetrization of Prochiral Cyclopentenes Enabled by Enantioselective Palladium-Catalyzed Oxidative Heck Reaction | 4.8 | 23 | Citations (PDF) |
| 67 | Palladium‐Catalyzed Enantioselective Cacchi Reaction: Asymmetric Synthesis of Axially Chiral 2,3‐Disubstituted Indoles | 14.4 | 170 | Citations (PDF) |
| 68 | Palladium‐Catalyzed Enantioselective Cacchi Reaction: Asymmetric Synthesis of Axially Chiral 2,3‐Disubstituted Indoles | 1.4 | 40 | Citations (PDF) |
| 69 | Construction of the Erythrinane Core Skeleton via Asymmetric Catalytic Cascade Reaction of Tertiary Enamides | 3.5 | 10 | Citations (PDF) |
| 70 | Asymmetric Total Synthesis of (−)-Arborisidine and (−)-19-epi-Arborisidine Enabled by a Catalytic Enantioselective Pictet–Spengler Reaction | 15.0 | 91 | Citations (PDF) |
| 71 | Radical‐Cation Cascade to Aryltetralin Cyclic Ether Lignans Under Visible‐Light Photoredox Catalysis | 1.4 | 2 | Citations (PDF) |
| 72 | Catalytic Enantioselective Synthesis and Switchable Chiroptical Property of Inherently Chiral Macrocycles | 15.0 | 146 | Citations (PDF) |
| 73 | Radical‐Cation Cascade to Aryltetralin Cyclic Ether Lignans Under Visible‐Light Photoredox Catalysis | 14.4 | 33 | Citations (PDF) |
| 74 | Palladium-Catalyzed Multicomponent Synthesis of Fully Substituted Alkylidene Furanones | 4.8 | 13 | Citations (PDF) |
| 75 | TiCl3‐Mediated Synthesis of 2,3,3‐Trisubstituted Indolenines: Total Synthesis of (+)‐1,2‐Dehydroaspidospermidine, (+)‐Condyfoline, and (−)‐Tubifoline | 1.4 | 8 | Citations (PDF) |
| 76 | TiCl3‐Mediated Synthesis of 2,3,3‐Trisubstituted Indolenines: Total Synthesis of (+)‐1,2‐Dehydroaspidospermidine, (+)‐Condyfoline, and (−)‐Tubifoline | 14.4 | 41 | Citations (PDF) |
| 77 | Synthesis of Benzo[a]carbazoles through Visible Light‐Induced Cycloaromatization | 1.8 | 2 | Citations (PDF) |
| 78 | Catalytic Enantioselective Benzilic Ester Rearrangement | 1.4 | 9 | Citations (PDF) |
| 79 | Copper‐Catalyzed Cyanoalkylative Aziridination of N‐Sulfonyl Allylamines | 3.8 | 11 | Citations (PDF) |
| 80 | Towards the Sarpagine‐Ajmaline‐Macroline Family of Indole Alkaloids: Enantioselective Synthesis of an N‐Demethyl Alstolactone Diastereomer | 3.4 | 15 | Citations (PDF) |
| 81 | Catalytic Enantioselective Benzilic Ester Rearrangement | 14.4 | 33 | Citations (PDF) |
| 82 | Functionalization of remote C(sp3)-H bonds enabled by copper-catalyzed coupling of O-acyloximes with terminal alkynes | 13.7 | 84 | Citations (PDF) |
| 83 | Construction of Quaternary Stereocenters by Palladium‐Catalyzed Carbopalladation‐Initiated Cascade Reactions | 1.4 | 66 | Citations (PDF) |
| 84 | Construction of Quaternary Stereocenters by Palladium‐Catalyzed Carbopalladation‐Initiated Cascade Reactions | 14.4 | 381 | Citations (PDF) |
| 85 | Remote C(sp<sup>3</sup>)−H Arylation and Vinylation of <i>N</i>‐Alkoxypyridinium Salts to δ‐Aryl and δ‐Vinyl Alcohols | 3.4 | 37 | Citations (PDF) |
| 86 | Catalytic Enantioselective Pinacol and Meinwald Rearrangements for the Construction of Quaternary Stereocenters | 15.0 | 93 | Citations (PDF) |
| 87 | Dual Photoredox/Copper Catalysis for the Remote C(sp<sup>3</sup>)−H Functionalization of Alcohols and Alkyl Halides by <i>N</i>‐Alkoxypyridinium Salts | 1.4 | 36 | Citations (PDF) |
| 88 | Formal [4+1] Cycloaddition of <i>o</i>‐Aminobenzyl Chlorides with Isocyanides: Synthesis of 2‐Amino‐3‐Substituted Indoles | 1.8 | 19 | Citations (PDF) |
| 89 | Recent Advances in Catalytic Enantioselective Rearrangement | 2.3 | 88 | Citations (PDF) |
| 90 | Copper‐Catalyzed 1,2‐Methoxy Methoxycarbonylation of Alkenes with Methyl Formate | 1.4 | 11 | Citations (PDF) |
| 91 | Copper‐Catalyzed 1,2‐Methoxy Methoxycarbonylation of Alkenes with Methyl Formate | 14.4 | 40 | Citations (PDF) |
| 92 | Catalytic Kinetic Resolution by Enantioselective Aromatization: Conversion of Racemic Intermediates of the Barton–Zard Reaction into Enantioenriched 3‐Arylpyrroles | 1.4 | 46 | Citations (PDF) |
| 93 | Catalytic Kinetic Resolution by Enantioselective Aromatization: Conversion of Racemic Intermediates of the Barton–Zard Reaction into Enantioenriched 3‐Arylpyrroles | 14.4 | 125 | Citations (PDF) |
| 94 | Iron‐Catalysed Remote C(sp<sup>3</sup>)−H Azidation of <i>O</i>‐Acyl Oximes and <i>N</i>‐Acyloxy Imidates Enabled by 1,5‐Hydrogen Atom Transfer of Iminyl and Imidate Radicals: Synthesis of γ‐Azido Ketones and β‐Azido Alcohols | 3.4 | 55 | Citations (PDF) |
| 95 | Intramolecular Arylation of Tertiary Enamides through Pd(OAc)<sub>2</sub>-Catalyzed Dehydrogenative Cross-Coupling Reaction: Construction of Fused <i>N</i>-Heterocyclic Scaffolds and Synthesis of Isoindolobenzazepine Alkaloids | 3.5 | 33 | Citations (PDF) |
| 96 | Copper-catalyzed remote C(sp3)–H azidation and oxidative trifluoromethylation of benzohydrazides | 13.7 | 99 | Citations (PDF) |
| 97 | Dual Photoredox/Copper Catalysis for the Remote C(sp<sup>3</sup>)−H Functionalization of Alcohols and Alkyl Halides by <i>N</i>‐Alkoxypyridinium Salts | 14.4 | 198 | Citations (PDF) |
| 98 | Stereoselective Total Synthesis of Eburnane‐Type Alkaloids Enabled by Conformation‐Directed Cyclization and Rearrangement | 14.4 | 68 | Citations (PDF) |
| 99 | Catalytic Atropenantioselective Heteroannulation between Isocyanoacetates and Alkynyl Ketones: Synthesis of Enantioenriched Axially Chiral 3‐Arylpyrroles | 1.4 | 53 | Citations (PDF) |
| 100 | Catalytic Atropenantioselective Heteroannulation between Isocyanoacetates and Alkynyl Ketones: Synthesis of Enantioenriched Axially Chiral 3‐Arylpyrroles | 14.4 | 164 | Citations (PDF) |
| 101 | Catalytic Enantioselective α‐Ketol Rearrangement | 1.4 | 17 | Citations (PDF) |
| 102 | Catalytic Enantioselective α‐Ketol Rearrangement | 14.4 | 38 | Citations (PDF) |
| 103 | Stereoselective Total Synthesis of Eburnane‐Type Alkaloids Enabled by Conformation‐Directed Cyclization and Rearrangement | 1.4 | 16 | Citations (PDF) |
| 104 | Heteroannulation of Arynes with α‐Amino Imides: Synthesis of 2,2‐Disubstituted Indolin‐3‐ones and Application to the Enantioselective Total Synthesis of (+)‐Hinckdentine A | 1.4 | 12 | Citations (PDF) |
| 105 | Copper‐Catalyzed Enantioselective Arylative Desymmetrization of Prochiral Cyclopentenes with Diaryliodonium Salts | 1.4 | 9 | Citations (PDF) |
| 106 | Copper‐Catalyzed Enantioselective Arylative Desymmetrization of Prochiral Cyclopentenes with Diaryliodonium Salts | 14.4 | 39 | Citations (PDF) |
| 107 | Palladium‐Catalyzed Enantioselective Desymmetrizing Aza‐Wacker Reaction: Development and Application to the Total Synthesis of (−)‐Mesembrane and (+)‐Crinane | 1.4 | 8 | Citations (PDF) |
| 108 | Palladium‐Catalyzed Enantioselective Desymmetrizing Aza‐Wacker Reaction: Development and Application to the Total Synthesis of (−)‐Mesembrane and (+)‐Crinane | 14.4 | 57 | Citations (PDF) |
| 109 | Still Unconquered: Enantioselective Passerini and Ugi Multicomponent Reactions | 17.0 | 230 | Citations (PDF) |
| 110 | Heteroannulation of Arynes with α‐Amino Imides: Synthesis of 2,2‐Disubstituted Indolin‐3‐ones and Application to the Enantioselective Total Synthesis of (+)‐Hinckdentine A | 14.4 | 78 | Citations (PDF) |
| 111 | Cooperative Pd/Cu Catalysis: Multicomponent Synthesis of Tetrasubstituted Imidazolones from Methyl α-Isocyanoacetates, Primary Amines, and Aryl(vinyl) Iodides | 4.8 | 32 | Citations (PDF) |
| 112 | Lewis acid catalyst-steered divergent synthesis of functionalized vicinal amino alcohols and pyrroles from tertiary enamides | 4.4 | 37 | Citations (PDF) |
| 113 | From isonitrile to nitrile via ketenimine intermediate: Palladium-catalyzed 1,1-carbocyanation of allyl carbonate by α-isocyanoacetate | 2.0 | 8 | Citations (PDF) |
| 114 | Copper-catalyzed methylative difunctionalization of alkenes | 13.7 | 89 | Citations (PDF) |
| 115 | Chiral phosphoric acid-catalyzed enantioselective three-component Mannich reaction of acyclic ketones, aldehydes and anilines | 2.0 | 10 | Citations (PDF) |
| 116 | Copper‐Catalyzed Arylation of Remote C(sp<sup>3</sup>)−H Bonds in Carboxamides and Sulfonamides | 1.4 | 38 | Citations (PDF) |
| 117 | Metamorphosis of cycloalkenes for the divergent total synthesis of polycyclic indole alkaloids | 37.7 | 168 | Citations (PDF) |
| 118 | Copper‐Catalyzed Arylation of Remote C(sp<sup>3</sup>)−H Bonds in Carboxamides and Sulfonamides | 14.4 | 186 | Citations (PDF) |
| 119 | Water as a Hydride Source in Palladium‐Catalyzed Enantioselective Reductive Heck Reactions | 1.4 | 158 | Citations (PDF) |
| 120 | Water as a Hydride Source in Palladium‐Catalyzed Enantioselective Reductive Heck Reactions | 14.4 | 193 | Citations (PDF) |
| 121 | Organocatalytic Nucleophilic Addition of Hydrazones to Imines: Synthesis of Enantioenriched Vicinal Diamines | 14.4 | 52 | Citations (PDF) |
| 122 | Fluorophores for Excited‐State Intramolecular Proton Transfer by an Yttrium Triflate Catalyzed Reaction of Isocyanides with Thiocarboxylic Acids | 14.4 | 42 | Citations (PDF) |
| 123 | Fluorophores for Excited‐State Intramolecular Proton Transfer by an Yttrium Triflate Catalyzed Reaction of Isocyanides with Thiocarboxylic Acids | 1.4 | 13 | Citations (PDF) |
| 124 | Organocatalytic Enantioselective Acyloin Rearrangement of α‐Hydroxy Acetals to α‐Alkoxy Ketones | 14.4 | 59 | Citations (PDF) |
| 125 | Rücktitelbild: Fluorophores for Excited‐State Intramolecular Proton Transfer by an Yttrium Triflate Catalyzed Reaction of Isocyanides with Thiocarboxylic Acids (Angew. Chem. 23/2017) | 1.4 | 2 | Citations (PDF) |
| 126 | Silver‐Catalyzed Three‐Component 1,1‐Aminoacylation of Homopropargylamines: α‐Additions for Both Terminal Alkynes and Isocyanides | 14.4 | 51 | Citations (PDF) |
| 127 | Organocatalytic Enantioselective Acyloin Rearrangement of α‐Hydroxy Acetals to α‐Alkoxy Ketones | 1.4 | 22 | Citations (PDF) |
| 128 | Organocatalytic Nucleophilic Addition of Hydrazones to Imines: Synthesis of Enantioenriched Vicinal Diamines | 1.4 | 17 | Citations (PDF) |
| 129 | Palladium‐Catalyzed Enantioselective Narasaka–Heck Reaction/Direct C−H Alkylation of Arenes: Iminoarylation of Alkenes | 14.4 | 115 | Citations (PDF) |
| 130 | Palladium‐Catalyzed Enantioselective Narasaka–Heck Reaction/Direct C−H Alkylation of Arenes: Iminoarylation of Alkenes | 1.4 | 34 | Citations (PDF) |
| 131 | Silver‐Catalyzed Three‐Component 1,1‐Aminoacylation of Homopropargylamines: α‐Additions for Both Terminal Alkynes and Isocyanides | 1.4 | 2 | Citations (PDF) |
| 132 | Palladium-Catalyzed Three-Component Reaction of Propargyl Carbonates, Isocyanides, and Alcohols or Water: Switchable Synthesis of Pyrroles and Its Bicyclic Analogues | 4.8 | 76 | Citations (PDF) |
| 133 | To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis | 37.7 | 401 | Citations (PDF) |
| 134 | Silver Nitrate-Catalyzed Isocyanide Insertion/Lactamization Sequence to Imidazolones and Quinazolin-4-ones: Development and Application in Natural Product Synthesis | 4.8 | 46 | Citations (PDF) |
| 135 | Catalytic Enantioselective Double Carbopalladation/C−H Functionalization with Statistical Amplification of Product Enantiopurity: A Convertible Linker Approach | 14.4 | 73 | Citations (PDF) |
| 136 | Catalytic Enantioselective Double Carbopalladation/C−H Functionalization with Statistical Amplification of Product Enantiopurity: A Convertible Linker Approach | 1.4 | 28 | Citations (PDF) |
| 137 | α‐Oxo‐Ketenimines from Isocyanides and α‐Haloketones: Synthesis and Divergent Reactivity | 3.4 | 25 | Citations (PDF) |
| 138 | Copper‐Catalyzed Enantioselective Domino Arylation/Semipinacol Rearrangement of Allylic Alcohols with Diaryliodonium Salts | 3.4 | 51 | Citations (PDF) |
| 139 | Copper‐Catalyzed Three‐Component Carboazidation of Alkenes with Acetonitrile and Sodium Azide | 1.4 | 39 | Citations (PDF) |
| 140 | Copper‐Catalyzed Three‐Component Carboazidation of Alkenes with Acetonitrile and Sodium Azide | 14.4 | 147 | Citations (PDF) |
| 141 | Copper‐Catalyzed Formal [2+2+1] Heteroannulation of Alkenes, Alkylnitriles, and Water: Method Development and Application to a Total Synthesis of (±)‐Sacidumlignan D | 14.4 | 68 | Citations (PDF) |
| 142 | Synthesis of Oxazolidin‐2‐ones by Oxidative Coupling of Isonitriles, Phenyl Vinyl Selenone, and Water | 3.4 | 32 | Citations (PDF) |
| 143 | Total Synthesis of (±)‐Strictamine | 1.4 | 25 | Citations (PDF) |
| 144 | Chiral Phosphoric Acid‐Catalyzed Enantioselective Formal [3+2] Cycloaddition of Azomethine Imines with Enecarbamates | 3.4 | 42 | Citations (PDF) |
| 145 | Enantioselective Total Syntheses of (−)‐Rhazinilam, (−)‐Leucomidine B, and (+)‐Leuconodine F | 1.4 | 17 | Citations (PDF) |
| 146 | Copper‐Catalyzed Formal [2+2+1] Heteroannulation of Alkenes, Alkylnitriles, and Water: Method Development and Application to a Total Synthesis of (±)‐Sacidumlignan D | 1.4 | 23 | Citations (PDF) |
| 147 | Chiral Phosphoric Acid Catalyzed Asymmetric Ugi Reaction by Dynamic Kinetic Resolution of the Primary Multicomponent Adduct | 14.4 | 108 | Citations (PDF) |
| 148 | Enantioselective Total Syntheses of (−)‐Rhazinilam, (−)‐Leucomidine B, and (+)‐Leuconodine F | 14.4 | 68 | Citations (PDF) |
| 149 | Catalytic Asymmetric Tandem Reaction of Tertiary Enamides: Expeditious Synthesis of Pyrrolo[2,1‐a]isoquinoline Alkaloid Derivatives | 14.4 | 62 | Citations (PDF) |
| 150 | Ketenimines from Isocyanides and Allyl Carbonates: Palladium‐Catalyzed Synthesis of β,γ‐Unsaturated Amides and Tetrazoles | 1.4 | 14 | Citations (PDF) |
| 151 | Synthesis of Diversely Functionalized Oxindoles Enabled by Migratory Insertion of Isocyanide to a Transient σ‐Alkylpalladium(II) Complex | 1.4 | 50 | Citations (PDF) |
| 152 | Synthesis of Diversely Functionalized Oxindoles Enabled by Migratory Insertion of Isocyanide to a Transient σ‐Alkylpalladium(II) Complex | 14.4 | 168 | Citations (PDF) |
| 153 | Enantioselective Synthesis of (+)-Peganumine A | 15.0 | 106 | Citations (PDF) |
| 154 | Copper-catalysed cyanoalkylative cycloetherification of alkenes to 1,3-dihydroisobenzofurans: development and application to the synthesis of citalopram | 3.4 | 55 | Citations (PDF) |
| 155 | Organocatalytic Enantioselective Vinylogous Pinacol Rearrangement Enabled by Chiral Ion Pairing | 1.4 | 25 | Citations (PDF) |
| 156 | Ketenimines from Isocyanides and Allyl Carbonates: Palladium‐Catalyzed Synthesis of β,γ‐Unsaturated Amides and Tetrazoles | 14.4 | 74 | Citations (PDF) |
| 157 | Organocatalytic Enantioselective Vinylogous Pinacol Rearrangement Enabled by Chiral Ion Pairing | 14.4 | 67 | Citations (PDF) |
| 158 | Enantioselective Synthesis of Quaternary α‐Amino Acids Enabled by the Versatility of the Phenylselenonyl Group | 3.4 | 21 | Citations (PDF) |
| 159 | Chiral Phosphoric Acid Catalyzed Asymmetric Ugi Reaction by Dynamic Kinetic Resolution of the Primary Multicomponent Adduct | 1.4 | 91 | Citations (PDF) |
| 160 | Total Synthesis of (±)‐Strictamine | 14.4 | 89 | Citations (PDF) |
| 161 | Enantioselective Total Synthesis of (−)‐Terengganensine A | 1.4 | 18 | Citations (PDF) |
| 162 | Switchable [3+2] and [4+2] Heteroannulation of Primary Propargylamines with Isonitriles to Imidazoles and 1,6‐Dihydropyrimidines: Catalyst Loading Enabled Reaction Divergence | 3.4 | 40 | Citations (PDF) |
| 163 | Catalytic Asymmetric Tandem Reaction of Tertiary Enamides: Expeditious Synthesis of Pyrrolo[2,1‐a]isoquinoline Alkaloid Derivatives | 1.4 | 8 | Citations (PDF) |
| 164 | Enantioselective Total Synthesis of (−)‐Terengganensine A | 14.4 | 69 | Citations (PDF) |
| 165 | Synthesis of Vinyl Isocyanides and Development of a Convertible Isonitrile | 4.8 | 36 | Citations (PDF) |
| 166 | Palladium-Catalyzed Enantioselective Domino Heck/Intermolecular C–H Bond Functionalization: Development and Application to the Synthesis of (+)-Esermethole | 15.0 | 192 | Citations (PDF) |
| 167 | Copper‐Catalyzed Intermolecular Carboetherification of Unactivated Alkenes by Alkyl Nitriles and Alcohols | 1.4 | 44 | Citations (PDF) |
| 168 | An Enantioselective Total Synthesis of (−)‐Isoschizogamine | 14.4 | 48 | Citations (PDF) |
| 169 | An Enantioselective Total Synthesis of (−)‐Isoschizogamine | 1.4 | 17 | Citations (PDF) |
| 170 | Aqueous Titanium Trichloride Promoted Reductive Cyclization of o‐Nitrostyrenes to Indoles: Development and Application to the Synthesis of Rizatriptan and Aspidospermidine | 14.4 | 117 | Citations (PDF) |
| 171 | Aqueous Titanium Trichloride Promoted Reductive Cyclization of o‐Nitrostyrenes to Indoles: Development and Application to the Synthesis of Rizatriptan and Aspidospermidine | 1.4 | 28 | Citations (PDF) |
| 172 | Enantioselective Synthesis of Putative Lipiarmycin Aglycon Related to Fidaxomicin/Tiacumicin B | 1.4 | 9 | Citations (PDF) |
| 173 | Tuning the Reactivity of Isocyano Group: Synthesis of Imidazoles and Imidazoliums from Propargylamines and Isonitriles in the Presence of Multiple Catalysts | 1.4 | 40 | Citations (PDF) |
| 174 | Copper‐Catalyzed Cyanomethylation of Allylic Alcohols with Concomitant 1,2‐Aryl Migration: Efficient Synthesis of Functionalized Ketones Containing an α‐Quaternary Center | 14.4 | 192 | Citations (PDF) |
| 175 | Copper‐Catalyzed Cyanomethylation of Allylic Alcohols with Concomitant 1,2‐Aryl Migration: Efficient Synthesis of Functionalized Ketones Containing an α‐Quaternary Center | 1.4 | 41 | Citations (PDF) |
| 176 | 2-(Methoxycarbonyl)ethyl as a Removable N-Protecting Group: Synthesis of Indoloisoquinolinones by Pd(II)-Catalyzed Intramolecular Diamination of Alkynes | 4.8 | 41 | Citations (PDF) |
| 177 | Copper‐Catalyzed Intermolecular Carboetherification of Unactivated Alkenes by Alkyl Nitriles and Alcohols | 14.4 | 161 | Citations (PDF) |
| 178 | Synthesis of diverse di- to penta-substituted 1,2-dihydropyridine derivatives from gold(I)-catalyzed intramolecular addition of tertiary enamides to alkynes | 1.4 | 40 | Citations (PDF) |
| 179 | Synthesis of Functionalized Epoxides by Copper-Catalyzed Alkylative Epoxidation of Allylic Alcohols with Alkyl Nitriles | 4.8 | 71 | Citations (PDF) |
| 180 | Total Syntheses of (−)-Mersicarpine, (−)-Scholarisine G, (+)-Melodinine E, (−)-Leuconoxine, (−)-Leuconolam, (−)-Leuconodine A, (+)-Leuconodine F, and (−)-Leuconodine C: Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon for Scholarisine G and Leuconodines A and C | 15.0 | 158 | Citations (PDF) |
| 181 | Pd/C‐Catalyzed Cyclizative Cross‐Coupling of Two ortho‐Alkynylanilines under Aerobic Conditions: Synthesis of 2,3′‐Bisindoles | 3.4 | 31 | Citations (PDF) |
| 182 | Sulfonamide and Tertiary Amine as Nucleophiles in Pd(II)-Catalyzed Diamination of Alkynes: Synthesis of Tetracyclic Indolobenzothiazine S,S-Dioxides | 4.8 | 32 | Citations (PDF) |
| 183 | Tuning the Reactivity of Isocyano Group: Synthesis of Imidazoles and Imidazoliums from Propargylamines and Isonitriles in the Presence of Multiple Catalysts | 14.4 | 107 | Citations (PDF) |
| 184 | Pd-Catalyzed Dehydrogenative Aryl–Aryl Bond Formation via Double C(sp2)–H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles | 4.8 | 73 | Citations (PDF) |
| 185 | Enantioselective Synthesis of Putative Lipiarmycin Aglycon Related to Fidaxomicin/Tiacumicin B | 14.4 | 44 | Citations (PDF) |
| 186 | Chiral Calcium–BINOL Phosphate Catalyzed Diastereo‐ and Enantioselective Synthesis of syn‐1,2‐Disubstituted 1,2‐Diamines: Scope and Mechanistic Studies | 3.4 | 42 | Citations (PDF) |
| 187 | Total Synthesis of (±)‐Aspidophylline A | 1.4 | 49 | Citations (PDF) |
| 188 | Phosphoric Acid Catalyzed Desymmetrization of Bicyclic Bislactones Bearing an All‐Carbon Stereogenic Center: Total Syntheses of (−)‐Rhazinilam and (−)‐Leucomidine B | 14.4 | 85 | Citations (PDF) |
| 189 | Phosphoric Acid Catalyzed Desymmetrization of Bicyclic Bislactones Bearing an All‐Carbon Stereogenic Center: Total Syntheses of (−)‐Rhazinilam and (−)‐Leucomidine B | 1.4 | 24 | Citations (PDF) |
| 190 | Phosphoric Acid Catalyzed Diastereo- and Enantioselective Synthesis of Substituted 1,3-Diaminotetralins | 4.8 | 25 | Citations (PDF) |
| 191 | Total Synthesis of (±)‐Aspidophylline A | 14.4 | 114 | Citations (PDF) |
| 192 | Chiral Phosphoric Acid‐Catalyzed Enantioselective Three‐ Component Aza‐Diels–Alder Reactions of Aminopyrroles and Aminopyrazoles | 3.8 | 41 | Citations (PDF) |
| 193 | NIS‐Assisted Aza‐Friedel–Crafts Reaction with α‐Carbamoysulfides as Precursors of N‐Carbamoylimines | 3.4 | 22 | Citations (PDF) |
| 194 | Copper-catalyzed three-component synthesis of 5-acetamidoimidazoles from carbodiimides, acyl chlorides and isocyanides | 4.4 | 30 | Citations (PDF) |
| 195 | Functionalized imidazoliniums from the three-component domino reaction of N-formylmethylcarboxamides with amines and isocyanides | 4.4 | 22 | Citations (PDF) |
| 196 | Copper‐Mediated/Catalyzed Oxyalkylation of Alkenes with Alkylnitriles | 3.4 | 95 | Citations (PDF) |
| 197 | Mechanistic Study on the Palladium(II)‐Catalyzed Synthesis of 2,3‐Disubstituted Indoles Under Aerobic Conditions: Anion Effects and the Development of a Low‐Catalyst‐Loading Process | 3.4 | 25 | Citations (PDF) |
| 198 | Triple Role of Phenylselenonyl Group Enabled a One-Pot Synthesis of 1,3-Oxazinan-2-ones From α-Isocyanoacetates, Phenyl Vinyl Selenones, and Water | 15.0 | 80 | Citations (PDF) |
| 199 | Unified Strategy to Monoterpene Indole Alkaloids: Total Syntheses of (±)-Goniomitine, (±)-1,2-Dehydroaspidospermidine, (±)-Aspidospermidine, (±)-Vincadifformine, and (±)-Kopsihainanine A | 15.0 | 147 | Citations (PDF) |
| 200 | Three-Component Povarov Reaction–Heteroannulation with Arynes: Synthesis of 5,6-Dihydroindolo[1,2-a]quinolines | 4.8 | 53 | Citations (PDF) |
| 201 | Plastidic type I signal peptidase 1 is a redox‐dependent thylakoidal processing peptidase | 6.2 | 21 | Citations (PDF) |
| 202 | Tertiary Amines as Synthetic Equivalents of Vinyl Cations: Zinc Bromide Promoted Coupling of Propargylamines with α‐Isocyanoacetamides To Give 2,4,5‐Trisubstituted Oxazoles Initiated by an Internal Redox Process | 3.4 | 19 | Citations (PDF) |
| 203 | Zinc Bromide Promoted Coupling of Isonitriles with Carboxylic Acids To Form 2,4,5‐Trisubstituted Oxazoles | 1.4 | 28 | Citations (PDF) |
| 204 | Palladium‐Catalyzed Decarboxylative Vinylation of Potassium Nitrophenyl Acetate: Application to the Total Synthesis of (±)‐Goniomitine | 14.4 | 100 | Citations (PDF) |
| 205 | Zinc Bromide Promoted Coupling of Isonitriles with Carboxylic Acids To Form 2,4,5‐Trisubstituted Oxazoles | 14.4 | 93 | Citations (PDF) |
| 206 | Palladium(II)‐Catalyzed Cyclizative Cross‐Coupling of ortho‐Alkynylanilines with ortho‐Alkynylbenzamides under Aerobic Conditions | 14.4 | 83 | Citations (PDF) |
| 207 | Synthesis of Multifunctionalized 1,2,3,4‐Tetrahydropyridines, 2,3‐Dihydropyridin‐4(1H)‐ones, and Pyridines from Tandem Reactions Initiated by [5+1] Cycloaddition of N‐Formylmethyl‐Substituted Enamides to Isocyanides: Mechanistic Insight and Synthetic Application | 3.4 | 34 | Citations (PDF) |
| 208 | Catalytic Enantioselective Michael Addition of α‐Aryl‐α‐Isocyanoacetates to Vinyl Selenone: Synthesis of α,α‐Disubstituted α‐Amino Acids and (+)‐ and (−)‐Trigonoliimine A | 14.4 | 133 | Citations (PDF) |
| 209 | Enantioselective Total Syntheses of Leuconolam–Leuconoxine–Mersicarpine Group Monoterpene Indole Alkaloids | 15.0 | 122 | Citations (PDF) |
| 210 | Palladium‐Catalyzed Through‐Space C(sp3)H and C(sp2)H Bond Activation by 1,4‐Palladium Migration: Efficient Synthesis of [3,4]‐Fused Oxindoles | 1.4 | 56 | Citations (PDF) |
| 211 | Palladium‐Catalyzed Through‐Space C(sp3)H and C(sp2)H Bond Activation by 1,4‐Palladium Migration: Efficient Synthesis of [3,4]‐Fused Oxindoles | 14.4 | 187 | Citations (PDF) |
| 212 | Heteroannulation of arynes with N-aryl-α-aminoketones for the synthesis of unsymmetrical N-aryl-2,3-disubstituted indoles: an aryne twist of Bischler–Möhlau indole synthesis | 3.4 | 54 | Citations (PDF) |
| 213 | From natural product to marketed drug: the tiacumicin odyssey | 10.6 | 90 | Citations (PDF) |
| 214 | Synthesis of Substituted Pyridines from Cascade [1 + 5] Cycloaddition of Isonitriles to N-Formylmethyl-Substituted Enamides, Aerobic Oxidative Aromatization, and Acyl Transfer Reaction | 15.0 | 182 | Citations (PDF) |
| 215 | Palladium‐Catalyzed Decarboxylative Vinylation of Potassium Nitrophenyl Acetate: Application to the Total Synthesis of (±)‐Goniomitine | 1.4 | 51 | Citations (PDF) |
| 216 | Pd(II)-catalyzed intramolecular aminopalladation/direct C–H arylation under aerobic conditions: synthesis of pyrrolo[1,2-a]indoles | 2.0 | 28 | Citations (PDF) |
| 217 | Ugi Four-Component Reaction of Alcohols: Stoichiometric and Catalytic Oxidation/MCR Sequences | 4.8 | 37 | Citations (PDF) |
| 218 | Synthesis of Iminonitriles by Oxone/TBAB-Mediated One-Pot Oxidative Three-Component Strecker Reaction | 2.3 | 27 | Citations (PDF) |
| 219 | Synthetic Study towards Strictamine: The Oxidative Coupling Approach | 1.4 | 30 | Citations (PDF) |
| 220 | Iron Chloride‐Catalyzed Three‐Component Domino Sequences: Syntheses of Functionalized α‐Oxy‐N‐acylhemiaminals and α‐Oxyimides | 3.8 | 20 | Citations (PDF) |
| 221 | Catalytic Enantioselective Michael Addition of α‐Aryl‐α‐Isocyanoacetates to Vinyl Selenone: Synthesis of α,α‐Disubstituted α‐Amino Acids and (+)‐ and (−)‐Trigonoliimine A | 1.4 | 51 | Citations (PDF) |
| 222 | Palladium(II)‐Catalyzed Cyclizative Cross‐Coupling of ortho‐Alkynylanilines with ortho‐Alkynylbenzamides under Aerobic Conditions | 1.4 | 31 | Citations (PDF) |
| 223 | Synthesis of 3,3-disubstituted oxindoles by one-pot integrated Brønsted base-catalyzed trichloroacetimidation of 3-hydroxyoxindoles and Brønsted acid-catalyzed nucleophilic substitution reaction | 2.6 | 44 | Citations (PDF) |
| 224 | Synthesis of Indoles by Copper-Catalyzed Heteroannulation of o-Aminophenylboronic Acid Pinacol Esters with β-Keto Esters | 2.3 | 11 | Citations (PDF) |
| 225 | Copper Catalyzed N-Arylation of Amidines with Aryl Boronic Acids and One-Pot Synthesis of Benzimidazoles by a Chan–Lam–Evans N-Arylation and C–H Activation/C–N Bond Forming Process | 4.8 | 104 | Citations (PDF) |
| 226 | Palladium‐Catalyzed Coupling of ortho‐Alkynylanilines with Terminal Alkynes Under Aerobic Conditions: Efficient Synthesis of 2,3‐Disubstituted 3‐Alkynylindoles | 1.4 | 52 | Citations (PDF) |
| 227 | Activation of a C(sp3)H Bond by a Transient σ‐Alkylpalladium(II) Complex: Synthesis of Spirooxindoles Through a Palladium‐Catalyzed Domino Carbopalladation/C(sp3)C(sp3) Bond‐Forming Process | 1.4 | 71 | Citations (PDF) |
| 228 | Palladium‐Catalyzed Coupling of ortho‐Alkynylanilines with Terminal Alkynes Under Aerobic Conditions: Efficient Synthesis of 2,3‐Disubstituted 3‐Alkynylindoles | 14.4 | 130 | Citations (PDF) |
| 229 | Activation of a C(sp3)H Bond by a Transient σ‐Alkylpalladium(II) Complex: Synthesis of Spirooxindoles Through a Palladium‐Catalyzed Domino Carbopalladation/C(sp3)C(sp3) Bond‐Forming Process | 14.4 | 197 | Citations (PDF) |
| 230 | Synthesis of 4-amino-1,2,3,4-tetrahydropyridine derivatives by intramolecular nucleophilic addition of tertiary enamides to in-situ generated imines | 2.0 | 32 | Citations (PDF) |
| 231 | Spirocyclization by Palladium-Catalyzed Domino Heck–Direct C–H Arylation Reactions: Synthesis of Spirodihydroquinolin-2-ones | 4.8 | 111 | Citations (PDF) |
| 232 | Organocatalytic Enantioselective One‐Pot Four‐Component Ugi‐Type Multicomponent Reaction for the Synthesis of Epoxy‐tetrahydropyrrolo[3,4‐b]pyridin‐5‐ones | 3.4 | 56 | Citations (PDF) |
| 233 | Amidation of Aldehydes and Alcohols through α‐Iminonitriles and a Sequential Oxidative Three‐Component Strecker Reaction/Thio‐Michael Addition/Alumina‐Promoted Hydrolysis Process to Access β‐Mercaptoamides from Aldehydes, Amines, and Thiols | 3.4 | 41 | Citations (PDF) |
| 234 | A Concise Total Synthesis of (±)-Trigonoliimine B | 4.8 | 47 | Citations (PDF) |
| 235 | Enantioselective Synthesis of 4‐Hydroxytetrahydropyridine Derivatives by Intramolecular Addition of Tertiary Enamides to Aldehydes | 1.4 | 10 | Citations (PDF) |
| 236 | Palladium(II)‐Catalyzed Intramolecular Diamination of Alkynes under Aerobic Oxidative Conditions: Catalytic Turnover of an Iodide Ion | 1.4 | 47 | Citations (PDF) |
| 237 | Enantioselective Synthesis of 4‐Hydroxytetrahydropyridine Derivatives by Intramolecular Addition of Tertiary Enamides to Aldehydes | 14.4 | 59 | Citations (PDF) |
| 238 | Palladium(II)‐Catalyzed Intramolecular Diamination of Alkynes under Aerobic Oxidative Conditions: Catalytic Turnover of an Iodide Ion | 14.4 | 157 | Citations (PDF) |
| 239 | Synergistic Effect of Palladium and Copper Catalysts: Catalytic Cyclizative Dimerization of ortho‐(1‐Alkynyl)benzamides Leading to Axially Chiral 1,3‐Butadienes | 3.4 | 62 | Citations (PDF) |
| 240 | Chiral Phosphoric Acid‐Catalyzed Enantioselective Three‐Component Povarov Reaction Using Cyclic Enethioureas as Dienophiles: Stereocontrolled Access to Enantioenriched Hexahydropyrroloquinolines | 3.4 | 83 | Citations (PDF) |
| 241 | Exploiting the Divergent Reactivity of Isocyanoacetates: One‐Pot Three‐Component Synthesis of Functionalized Angular Furoquinolines | 2.3 | 22 | Citations (PDF) |
| 242 | Iodo-Carbocyclization of Electron-Deficient Alkenes: Synthesis of Oxindoles and Spirooxindoles | 4.8 | 112 | Citations (PDF) |
| 243 | Chiral Calcium Organophosphate-Catalyzed Enantioselective Electrophilic Amination of Enamides | 4.8 | 86 | Citations (PDF) |
| 244 | Chiral Phosphoric Acid-Catalyzed Enantioselective Three-Component Povarov Reaction Using Enecarbamates as Dienophiles: Highly Diastereo- and Enantioselective Synthesis of Substituted 4-Aminotetrahydroquinolines | 15.0 | 270 | Citations (PDF) |
| 245 | Unexpected C–C Bond Cleavage: Synthesis of 1,2,4-Oxadiazol-5-ones from Amidoximes with Pentafluorophenyl or Trifluoromethyl Anion Acting as Leaving Group | 4.8 | 33 | Citations (PDF) |
| 246 | Trifluoroacetic Acid-Promoted Synthesis of 3-Hydroxy, 3-Amino and Spirooxindoles from α-Keto-N-Anilides | 4.8 | 71 | Citations (PDF) |
| 247 | A Practical, One‐Pot Multicomponent Synthesis of α‐Amidosulfides and Their Application as Latent N‐Acylimines in the Friedel–Crafts Reaction | 2.3 | 26 | Citations (PDF) |
| 248 | Protecting‐Group‐Free Total Synthesis of (E)‐ and (Z)‐Alstoscholarine | 1.4 | 14 | Citations (PDF) |
| 249 | Cinchona Alkaloid Amide Catalyzed Enantioselective Formal [2+2] Cycloadditions of Allenoates and Imines: Synthesis of 2,4‐Disubstituted Azetidines | 1.4 | 33 | Citations (PDF) |
| 250 | Protecting‐Group‐Free Total Synthesis of (E)‐ and (Z)‐Alstoscholarine | 14.4 | 58 | Citations (PDF) |
| 251 | Cinchona Alkaloid Amide Catalyzed Enantioselective Formal [2+2] Cycloadditions of Allenoates and Imines: Synthesis of 2,4‐Disubstituted Azetidines | 14.4 | 117 | Citations (PDF) |
| 252 | Exploiting the Divergent Reactivity of α‐Isocyanoacetate: Multicomponent Synthesis of 5‐Alkoxyoxazoles and Related Heterocycles | 3.4 | 77 | Citations (PDF) |
| 253 | Synthesis of Hydroxylated 3,4-Dihydropyridine-2-ones from Intramolecular Nucleophilic Addition Reaction of Oxirane-Containing Tertiary Enamides | 1.4 | 3 | Citations (PDF) |
| 254 | Asymmetric Synthesis of 2,4,6-Trideoxy-4-(dimethylamino)-3-C-methyl-l-lyxohexopyranose (Lemonose) | 1.4 | 2 | Citations (PDF) |
| 255 | Simulation of fruit-set and trophic competition and optimization of yield advantages in six Capsicum cultivars using functional–structural plant modelling | 3.1 | 25 | Citations (PDF) |
| 256 | Palladium-Catalyzed Carbo-Heterofunctionalization of Alkenes for the Synthesis of Oxindoles and Spirooxindoles | 4.8 | 196 | Citations (PDF) |
| 257 | Hybridization of Long Pyridine‐Dicarboxamide Oligomers into Multi‐Turn Double Helices: Slow Strand Association and Dissociation, Solvent Dependence, and Solid State Structures | 3.0 | 63 | Citations (PDF) |
| 258 | Efficient Synthesis of α-Ketoamides via 2-Acyl-5-aminooxazoles by Reacting Acyl Chlorides and α-Isocyanoacetamides | 4.8 | 82 | Citations (PDF) |
| 259 | Enantioselective Aza‐Morita–Baylis–Hillman Reaction Using Aliphatic α‐Amidosulfones as Imine Surrogates | 3.8 | 50 | Citations (PDF) |
| 260 | Palladium‐Catalyzed Domino Process to Spirooxindoles: Ligand Effect on Aminopalladation versus Carbopalladation | 3.4 | 86 | Citations (PDF) |
| 261 | Intramolecular Suzuki–Miyaura Reaction for the Total Synthesis of Signal Peptidase Inhibitors, Arylomycins A2 and B2 | 3.4 | 53 | Citations (PDF) |
| 262 | Total Synthesis of Complestatin (Chloropeptin II) | 1.4 | 9 | Citations (PDF) |
| 263 | Total Synthesis of Complestatin (Chloropeptin II) | 14.4 | 54 | Citations (PDF) |
| 264 | Palladium-catalyzed domino Heck/cyanation: synthesis of 3-cyanomethyloxindoles and their conversion to spirooxoindoles | 2.0 | 61 | Citations (PDF) |
| 265 | Passerini Three-Component Reaction of Alcohols under Catalytic Aerobic Oxidative Conditions | 4.8 | 84 | Citations (PDF) |
| 266 | Copper-promoted N-cyclopropylation of anilines and amines by cyclopropylboronic acid | 3.4 | 54 | Citations (PDF) |
| 267 | IBX/TBAB-Mediated Oxidation of Primary Amines to Nitriles | 2.3 | 3 | Citations (PDF) |
| 268 | Combination of Lithium Chloride and Hexafluoroisopropanol for Friedel-Crafts Reactions | 1.4 | 9 | Citations (PDF) |
| 269 | Total Synthesis of Horsfiline: A Palladium-Catalyzed Domino Heck-Cyanation Strategy | 1.4 | 8 | Citations (PDF) |
| 270 | Synthesis of l-3-Hydroxy-4-methoxy-5-methylphenylalanol | 1.4 | 2 | Citations (PDF) |
| 271 | Palladium‐Catalyzed Annulation of Acyloximes with Arynes (or Alkynes): Synthesis of Phenanthridines and Isoquinolines | 1.4 | 80 | Citations (PDF) |
| 272 | Brønsted Acid Catalyzed Enantioselective Three‐Component Reaction Involving the α Addition of Isocyanides to Imines | 1.4 | 50 | Citations (PDF) |
| 273 | Palladium‐Catalyzed Annulation of Acyloximes with Arynes (or Alkynes): Synthesis of Phenanthridines and Isoquinolines | 14.4 | 304 | Citations (PDF) |
| 274 | Brønsted Acid Catalyzed Enantioselective Three‐Component Reaction Involving the α Addition of Isocyanides to Imines | 14.4 | 175 | Citations (PDF) |
| 275 | Palladium-catalyzed domino N-arylation/carbopalladation/C–H functionalization: three-component synthesis of 3-(diarylmethylene)oxindoles | 1.4 | 56 | Citations (PDF) |
| 276 | Chiral Brønsted Acid-Catalyzed Enantioselective Three-Component Povarov Reaction | 15.0 | 400 | Citations (PDF) |
| 277 | Synthesis of Pyrroles by Consecutive Multicomponent Reaction/[4 + 1] Cycloaddition of α-Iminonitriles with Isocyanides | 4.8 | 114 | Citations (PDF) |
| 278 | Ugi-Post Functionalization, from a Single Set of Ugi-Adducts to Two Distinct Heterocycles by Microwave-Assisted Palladium-Catalyzed Cyclizations: Tuning the Reaction Pathways by Ligand Switch | 3.5 | 101 | Citations (PDF) |
| 279 | Asymmetric Total Syntheses of (−)-Renieramycin M and G and (−)-Jorumycin Using Aziridine as a Lynchpin | 4.8 | 98 | Citations (PDF) |
| 280 | Chiral Brønsted Acid-Catalyzed Enantioselective Multicomponent Mannich Reaction: Synthesis of anti-1,3-Diamines Using Enecarbamates as Nucleophiles | 4.8 | 120 | Citations (PDF) |
| 281 | Invertible Enantioselectivity in 6′-Deoxy-6′-acylamino-β-isocupreidine-Catalyzed Asymmetric Aza-Morita−Baylis−Hillman Reaction: Key Role of Achiral Additive | 4.8 | 82 | Citations (PDF) |
| 282 | Synthetic Studies on (−)-Lemonomycin: An Efficient Asymmetric Synthesis of Lemonomycinone Amide | 3.5 | 39 | Citations (PDF) |
| 283 | Catalytic Enantioselective Passerini Three‐Component Reaction | 14.4 | 144 | Citations (PDF) |
| 284 | Synthesis of α‐Ketoamides by a Molecular‐Sieves‐Promoted Formal Oxidative Coupling of Aliphatic Aldehydes with Isocyanides | 14.4 | 99 | Citations (PDF) |
| 285 | Synthesis of Diastereomers of Complestatin and Chloropeptin I: Substrate‐Dependent Atropstereoselectivity of the Intramolecular Suzuki–Miyaura Reaction | 14.4 | 65 | Citations (PDF) |
| 286 | Asymmetric Synthesis of 5‐(1‐Hydroxyalkyl)tetrazoles by Catalytic Enantioselective Passerini‐Type Reactions | 14.4 | 128 | Citations (PDF) |
| 287 | Catalytic Enantioselective Passerini Three‐Component Reaction | 1.4 | 45 | Citations (PDF) |
| 288 | Synthesis of α‐Ketoamides by a Molecular‐Sieves‐Promoted Formal Oxidative Coupling of Aliphatic Aldehydes with Isocyanides | 1.4 | 25 | Citations (PDF) |
| 289 | Synthesis of Diastereomers of Complestatin and Chloropeptin I: Substrate‐Dependent Atropstereoselectivity of the Intramolecular Suzuki–Miyaura Reaction | 1.4 | 14 | Citations (PDF) |
| 290 | Asymmetric Synthesis of 5‐(1‐Hydroxyalkyl)tetrazoles by Catalytic Enantioselective Passerini‐Type Reactions | 1.4 | 30 | Citations (PDF) |
| 291 | Palladium-Catalyzed Domino Intramolecular N-Arylation/Intermolecular C−C Bond Formation for the Synthesis of Functionalized Benzodiazepinediones | 4.8 | 67 | Citations (PDF) |
| 292 | One-Pot Three-Component Synthesis of α-Iminonitriles by IBX/TBAB-Mediated Oxidative Strecker Reaction | 4.8 | 112 | Citations (PDF) |
| 293 | Highly Enantioselective Aza Morita−Baylis−Hillman Reaction Catalyzed by Bifunctional β-Isocupreidine Derivatives | 15.0 | 113 | Citations (PDF) |
| 294 | Asymmetric Total Synthesis of (−)-Quinocarcin | 15.0 | 82 | Citations (PDF) |
| 295 | Total Synthesis of Arylomycin
A2, a Signal Peptidase I (SPase I) Inhibitor | 1.4 | 5 | Citations (PDF) |
| 296 | Dolichol Biosynthesis and Its Effects on the Unfolded Protein Response and Abiotic Stress Resistance in Arabidopsis | 7.6 | 113 | Citations (PDF) |
| 297 | Synthesis of dihydrophenanthridines by a sequence of Ugi-4CR and palladium-catalyzed intramolecular C-H functionalization | 1.9 | 23 | Citations (PDF) |
| 298 | Lithium Bromide-Promoted Three-Component Synthesis of Oxa-Bridged Tetracyclic Tetrahydroisoquinolines | 0.4 | 21 | Citations (PDF) |
| 299 | Synthesis of Protected Chiral Vicinal Diaminoalcohols by Diastereoselective Intramolecular Benzylic Substitution from Bistrichloroacetimidates | 4.8 | 19 | Citations (PDF) |
| 300 | Chiral Salen−Aluminum Complex as a Catalyst for Enantioselective α-Addition of Isocyanides to Aldehydes: Asymmetric Synthesis of 2-(1-Hydroxyalkyl)-5-aminooxazoles | 4.8 | 111 | Citations (PDF) |
| 301 | Synthesis of DEFG Ring of Complestatin and Chloropeptin I: Highly Atropdiastereoselective Macrocyclization by Intramolecular Suzuki-Miyaura Reaction | 4.8 | 64 | Citations (PDF) |
| 302 | Ammonium Chloride Promoted Three-Component Synthesis of 5-Iminooxazoline and Its Subsequent Transformation to Macrocyclodepsipeptide | 4.8 | 76 | Citations (PDF) |
| 303 | Palladium-Catalyzed Enantioselective Domino Heck–Cyanation Sequence: Development and Application to the Total Synthesis of Esermethole and Physostigmine | 3.4 | 269 | Citations (PDF) |
| 304 | The Enantioselective Morita–Baylis–Hillman Reaction and Its Aza Counterpart | 14.4 | 474 | Citations (PDF) |
| 305 | Modulating the Reactivity of α-Isocyanoacetates: Multicomponent Synthesis of 5-Methoxyoxazoles and Furopyrrolones | 14.4 | 178 | Citations (PDF) |
| 306 | Palladium-Catalyzed Three-Component Synthesis of 3-(Diarylmethylene)oxindoles through a Domino Sonagashira/Carbopalladation/CH Activation/CC Bond-Forming Sequence | 14.4 | 185 | Citations (PDF) |
| 307 | Total Synthesis of the Marine Natural Product (−)-Cribrostatin 4 (Renieramycin H) | 14.4 | 48 | Citations (PDF) |
| 308 | IBX-Mediated Oxidative Ugi-Type Multicomponent Reactions: Application to the N and C1 Functionalization of Tetrahydroisoquinoline | 14.4 | 169 | Citations (PDF) |
| 309 | Enantioselektive Morita-Baylis-Hillman-Reaktionen und ihre Aza-Varianten | 1.4 | 98 | Citations (PDF) |
| 310 | Modulating the Reactivity of α-Isocyanoacetates: Multicomponent Synthesis of 5-Methoxyoxazoles and Furopyrrolones | 1.4 | 51 | Citations (PDF) |
| 311 | Palladium-Catalyzed Three-Component Synthesis of 3-(Diarylmethylene)oxindoles through a Domino Sonagashira/Carbopalladation/CH Activation/CC Bond-Forming Sequence | 1.4 | 57 | Citations (PDF) |
| 312 | Total Synthesis of the Marine Natural Product (−)-Cribrostatin 4 (Renieramycin H) | 1.4 | 3 | Citations (PDF) |
| 313 | IBX-Mediated Oxidative Ugi-Type Multicomponent Reactions: Application to the N and C1 Functionalization of Tetrahydroisoquinoline | 1.4 | 26 | Citations (PDF) |
| 314 | Asymmetric Lewis Acid Catalyzed Addition of Isocyanides to Aldehydes – Synthesis of 5-Amino-2-(1-hydroxyalkyl)oxazoles | 2.3 | 83 | Citations (PDF) |
| 315 | Total Synthesis of Ecteinascidin 743 | 15.0 | 170 | Citations (PDF) |
| 316 | Synthesis of 3-(Diarylmethylenyl)oxindole by a Palladium-Catalyzed Domino Carbopalladation/C−H Activation/C−C Bond-Forming Process | 4.8 | 182 | Citations (PDF) |
| 317 | Palladium-Catalyzed, Modular Synthesis of Highly Functionalized Indoles and Tryptophans by Direct Annulation of Substitutedo-Haloanilines and Aldehydes | 3.5 | 135 | Citations (PDF) |
| 318 | Rapid Access to Oxindoles by the Combined Use of an Ugi Four-Component Reaction and a Microwave-Assisted Intramolecular Buchwald−Hartwig Amidation Reaction | 4.8 | 152 | Citations (PDF) |
| 319 | Aziridinium fromN,N-Dibenzyl Serine Methyl Ester: Synthesis of Enantiomerically Pure β-Amino and α,β-Diamino Esters | 4.8 | 45 | Citations (PDF) |
| 320 | One-Pot Synthesis of Macrocycles by a Tandem Three-Component Reaction and Intramolecular [3+2] Cycloaddition | 4.8 | 136 | Citations (PDF) |
| 321 | Nomenclature for HKT transporters, key determinants of plant salinity tolerance | 11.6 | 372 | Citations (PDF) |
| 322 | Rapid Synthesis of Cyclopeptide Alkaloid-Likepara-Cyclophanes by Combined Use of Ugi-4CR and Intramolecular SNAr Reaction | 1.3 | 25 | Citations (PDF) |
| 323 | Importance of the Structure of Vancomycin Binding Pocket in Designing Compounds Active Against Vancomycin-resistant Enterococci (VRE) | 2.4 | 3 | Citations (PDF) |
| 324 | 5-Aminooxazole as an Internal Traceless Activator of C-Terminal Carboxylic Acid: Rapid Access to Diversely Functionalized Cyclodepsipeptides | 3.4 | 34 | Citations (PDF) |
| 325 | Design and Synthesis of Simple Macrocycles Active Against Vancomycin-ResistantEnterococci (VRE) | 3.4 | 11 | Citations (PDF) |
| 326 | Alcohols in Isonitrile-Based Multicomponent Reaction: Passerini Reaction of Alcohols in the Presence ofO-Iodoxybenzoic Acid | 14.4 | 105 | Citations (PDF) |
| 327 | Asymmetric Total Syntheses of Ecteinascidin 597 and Ecteinascidin 583 | 14.4 | 44 | Citations (PDF) |
| 328 | Alcohols in Isonitrile-Based Multicomponent Reaction: Passerini Reaction of Alcohols in the Presence ofO-Iodoxybenzoic Acid | 1.4 | 28 | Citations (PDF) |
| 329 | Asymmetric Total Syntheses of Ecteinascidin 597 and Ecteinascidin 583 | 1.4 | 9 | Citations (PDF) |
| 330 | Mono Alkylation of α-Isocyano Acetamide to its Higher Homologues | 1.4 | 7 | Citations (PDF) |
| 331 | Synthetic Studies on Ecteinascidin 743 (Et 743): Asymmetric Synthesis of a Highly Oxygenated Tetrahydroisoquinoline via a Key Phenolic Mannich Reaction | 2.3 | 4 | Citations (PDF) |
| 332 | Synthesis of 4-Nitrophenyl Sulfones and Application in the Modified Julia Olefination | 1.4 | 3 | Citations (PDF) |
| 333 | Synthetic Studies towards (-)-Lemonomycin, Synthesis of Fused Tetracycles | 1.4 | 3 | Citations (PDF) |
| 334 | Multicomponent synthesis of epoxy-tetrahydronaphthyridine and structural diversification by subsequent fragmentation | 2.0 | 16 | Citations (PDF) |
| 335 | Identification of synthetic compounds active against VRE: the role of the lipidated aminoglucose and the structure of glycopeptide binding pocket | 2.0 | 6 | Citations (PDF) |
| 336 | Conformation‐Directed Macrocyclization Reactions | 2.3 | 193 | Citations (PDF) |
| 337 | Total Synthesis of Mauritines A, B, C, and F: Cyclopeptide Alkaloids with a 14-Membered Paracyclophane Unit | 3.4 | 30 | Citations (PDF) |
| 338 | Design and synthesis of macrocycles active against vancomycin-resistant enterococci (VRE): the interplay between d-Ala-d-Lac binding and hydrophobic effect | 2.0 | 8 | Citations (PDF) |
| 339 | Asymmetric Synthesis of Protected γ-Carboxy-l-glutamic Acid | 1.4 | 0 | Citations (PDF) |
| 340 | A Three-Component Synthesis of (1,3-Oxazol-2-yl)-1,2-dihydro(iso)quinoline and its further Structural Diversifications | 1.4 | 1 | Citations (PDF) |
| 341 | Synthesis of Ring-A-Substituted Tryptophan by a Palladium-Catalyzed Heteroannulation Reaction | 1.4 | 3 | Citations (PDF) |
| 342 | Synthesis of α-Isocyano-α-alkyl(aryl)acetamides and their Use in the Multicomponent Synthesis of 5-Aminooxazole, Pyrrolo[3,4-b]pyridin-5-one and 4,5,6,7-Tetrahydrofuro[2,3-c]pyridine | 2.3 | 6 | Citations (PDF) |
| 343 | Mild Oxidative One-Carbon Homologation of Aldehyde to Amide | 15.0 | 60 | Citations (PDF) |
| 344 | Three-Component Synthesis of Polysubstituted 6-Azaindolines and Its Tricyclic Derivatives | 4.8 | 91 | Citations (PDF) |
| 345 | Microwave-Assisted Intramolecular Suzuki−Miyaura Reaction to Macrocycle, a Concise Asymmetric Total Synthesis of Biphenomycin B | 4.8 | 71 | Citations (PDF) |
| 346 | Synthesis of Chiral Vicinal Diamines by Highly Diastereoselective Three-Component Phenolic Mannich Reaction: Temperature-Dependent Stereodivergency | 4.8 | 51 | Citations (PDF) |
| 347 | Exploiting the Dual Reactivity ofo-Isocyanobenzamide: Three-Component Synthesis of 4-Imino-4H-3,1-benzoxazines | 4.8 | 57 | Citations (PDF) |
| 348 | Synthetic Studies toward Ecteinascidin 743 | 3.5 | 72 | Citations (PDF) |
| 349 | A Short Enantioselective Synthesis of Protectedl-3-Hydroxy-4-methoxy-5-methyl Phenylalanine and its Corresponding Aldehyde - A Common Subunit of Ecteinascidin-743, Safracin and Congeners | 1.4 | 2 | Citations (PDF) |
| 350 | Synthesis of Polysubstituted 4,5,6,7-Tetrahydrofuro[2,3-c]pyridines by a Novel Multicomponent Reaction | 4.8 | 80 | Citations (PDF) |
| 351 | Reeve's synthesis of 2-imino-4-thiazolidinone from alkyl (aryl) trichloromethylcarbinol revisited, a three-component process from aldehyde, chloroform and thiourea | 1.4 | 52 | Citations (PDF) |
| 352 | Truncated diastereoselective Passerini reaction, a rapid construction of polysubstituted oxazole and peptides having an α-hydroxy-β-amino acid component | 2.0 | 61 | Citations (PDF) |
| 353 | Strained-Cyclophane-Induced β-Turn Template: Design, Synthesis, and Spectroscopic Characterization | 4.8 | 22 | Citations (PDF) |
| 354 | Ammonium Chloride Promoted Ugi Four-Component, Five-Center Reaction of α-Substituted α-Isocyano Acetic Acid: A Strong Solvent Effect | 4.8 | 46 | Citations (PDF) |
| 355 | Palladium- and Copper-Catalyzed Synthesis of Medium- and Large-Sized Ring-Fused Dihydroazaphenanthrenes and 1,4-Benzodiazepine-2,5-diones. Control of Reaction Pathway by Metal-Switching | 15.0 | 150 | Citations (PDF) |
| 356 | A Short Synthesis of (-)-Deoxoprosophylline | 0.4 | 22 | Citations (PDF) |
| 357 | Recent Developments in the Isonitrile‐Based Multicomponent Synthesis of Heterocycles | 2.3 | 916 | Citations (PDF) |
| 358 | One-Pot Synthesis of Polyheterocycles by a Palladium-Catalyzed Intramolecular N-Arylation/CH Activation/Aryl–Aryl Bond-Forming Domino Process | 1.4 | 26 | Citations (PDF) |
| 359 | Total Synthesis of an Atropdiastereomer of RP-66453 and Determination of Its Absolute Configuration | 1.4 | 17 | Citations (PDF) |
| 360 | Title is missing! | 1.4 | 32 | Citations (PDF) |
| 361 | One-Pot Synthesis of Polyheterocycles by a Palladium-Catalyzed Intramolecular N-Arylation/CH Activation/Aryl–Aryl Bond-Forming Domino Process | 14.4 | 73 | Citations (PDF) |
| 362 | Total Synthesis of an Atropdiastereomer of RP-66453 and Determination of Its Absolute Configuration | 14.4 | 58 | Citations (PDF) |
| 363 | A One-Pot Four-Component (ABC2) Synthesis of Macrocycles | 14.4 | 102 | Citations (PDF) |
| 364 | Rapid and diverse route to natural product-like biaryl ether containing macrocycles | 2.0 | 102 | Citations (PDF) |
| 365 | Solid-phase synthesis of natural product-like macrocycles by a sequence of Ugi-4CR and SNAr-based cycloetherification | 1.4 | 48 | Citations (PDF) |
| 366 | Synthetic studies on ecteinascidin 743: rapid access to the fully functionalized tetrahydroisoquinoline with a bridged 10-membered sulfur containing macrocycleElectronic supplementary information (ESI) available: spectroscopic data for all new compounds and X-ray data for compound 14. See http://www.rsc.org/suppdata/cc/b3/b309824a/ | 3.4 | 29 | Citations (PDF) |
| 367 | From central to planar chirality, the first example of atropenantioselective cycloetherification | 2.6 | 49 | Citations (PDF) |
| 368 | allo-Aromadendrane- and Picrotoxane-Type Sesquiterpenes fromDendrobium moniliforme | 0.4 | 35 | Citations (PDF) |
| 369 | Asymmetric Synthesis of OrthogonallyProtected (2S,4R)-and (2S,4S)-4-Hydroxyornithine | 1.4 | 0 | Citations (PDF) |
| 370 | Synthesis of Isocyano Peptidesby Dehydration of theN-Formyl Derivatives | 1.4 | 12 | Citations (PDF) |
| 371 | N-Carbamate-Assisted Stereoselective Synthesis of Chiral Vicinal Amino Sulfides | 4.8 | 27 | Citations (PDF) |
| 372 | Ammonium Chloride-Promoted Four-Component Synthesis of Pyrrolo[3,4-b]pyridin-5-one | 15.0 | 212 | Citations (PDF) |
| 373 | A Convergent Approach to Cyclopeptide Alkaloids: Total Synthesis of Sanjoinine G1 | 15.0 | 69 | Citations (PDF) |
| 374 | Rapid access to tetracyclic ring system of lennoxamine type natural product by combined use of a novel three-component reaction and Pummerer cyclization | 3.4 | 35 | Citations (PDF) |
| 375 | Title is missing! | 1.4 | 38 | Citations (PDF) |
| 376 | Title is missing! | 1.4 | 27 | Citations (PDF) |
| 377 | Synthesis of Furoquinolines by a Multicomponent Domino Process | 14.4 | 108 | Citations (PDF) |
| 378 | A Five-Component Synthesis of Hexasubstituted Benzene | 14.4 | 88 | Citations (PDF) |
| 379 | Multicomponent domino process to oxa-bridged polyheterocycles and pyrrolopyridines, structural diversity derived from work-up procedure | 2.0 | 64 | Citations (PDF) |
| 380 | Studies toward the total synthesis of RP-66453 | 1.4 | 22 | Citations (PDF) |
| 381 | Three component synthesis of oxa-bridged tetracyclic tetrahydroquinolines | 3.4 | 62 | Citations (PDF) |
| 382 | A Novel Multicomponent Synthesis of Polysubstituted 5-Aminooxazole and Its New Scaffold-Generating Reaction to Pyrrolo[3,4-b]pyridine | 4.8 | 188 | Citations (PDF) |
| 383 | Studies on the Total Synthesis of RP 66453: Synthesis of Fully Functionalized 15-Membered Biaryl-Containing Macrocycle | 4.8 | 44 | Citations (PDF) |
| 384 | A Rapid Access to Biaryl Ether Containing Macrocycles by Pairwise Use of Ugi 4CR and Intramolecular SNAr-Based Cycloetherification | 4.8 | 85 | Citations (PDF) |
| 385 | Activation of a Terminal Carboxylic Acid by an Internal Oxazole: A Novel Synthesis of Macrocyclodepsipeptide | 15.0 | 77 | Citations (PDF) |
| 386 | An autoxidative approach to 1,2,3,4-tetrahydroisoquinolin-1-one and tetrahydro-β-carbolin-1-one | 1.4 | 10 | Citations (PDF) |
| 387 | Asymmetric total synthesis of (−)-deoxoprosophylline | 1.4 | 28 | Citations (PDF) |
| 388 | Diethyl oxomalonate as a three carbon synthon for synthesis of functionalized 1,1′-disubstituted tetrahydroisoquinoline | 1.4 | 17 | Citations (PDF) |
| 389 | Synthesis of a model 22-membered AB-C-O-D ring of vancomycin containing biaryl and biaryl ether linkages | 1.4 | 13 | Citations (PDF) |
| 390 | An efficient total synthesis of K-13, a non-competitive inhibitor of ACE I | 1.4 | 18 | Citations (PDF) |
| 391 | The first total synthesis of mauritine-A | 1.4 | 23 | Citations (PDF) |
| 392 | An efficient stereoselective and stereodivergent synthesis of (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids | 1.4 | 44 | Citations (PDF) |
| 393 | RECENT PROGRESS IN ISOLATION, BIOACTIVITY EVALUATION AND TOTAL SYNTHESIS OF DIARYLHEPTANOIDS | 1.9 | 41 | Citations (PDF) |
| 394 | Asymmetric Synthesis of Actinoidic Acid Derivatives | 4.8 | 28 | Citations (PDF) |
| 395 | A Novel Synthesis of Biaryl-Containing Macrocycles by a Domino Miyaura Arylboronate Formation: Intramolecular Suzuki Reaction | 4.8 | 96 | Citations (PDF) |
| 396 | A convenient one-step synthesis of mono-N-functionalized tetraazamacrocycles | 1.0 | 27 | Citations (PDF) |
| 397 | A convenient synthesis of bis-tetraazamacrocycles | 1.4 | 10 | Citations (PDF) |
| 398 | An asymmetric total synthesis of sanjoinine G1 | 1.4 | 25 | Citations (PDF) |
| 399 | Design and synthesis of novel tridentate and tetradentate chiral ligands | 1.4 | 6 | Citations (PDF) |
| 400 | A high throughput synthesis of aryl triflate and aryl nonaflate promoted by a polymer supported base (PTBD) | 1.4 | 33 | Citations (PDF) |
| 401 | Total synthesis and conformational studies of hapalosin, N-desmethylhapalosin and 8-Deoxyhapalosin1Dedicated with affection and respect to the memory of Professor Sir Derek H. R. Barton in recognition of his distinguished contributions to science and in sincere gratitude for the immense degree of inspiration and encouragement he provided to one of us (J. Zhu).1 | 2.6 | 31 | Citations (PDF) |
| 402 | Total Synthesis of an Antitumor Agent RA-VII via an Efficient Preparation of Cycloisodityrosine† | 3.5 | 52 | Citations (PDF) |
| 403 | Recent developments in reversing glycopeptide-resistant pathogens | 3.9 | 39 | Citations (PDF) |
| 404 | A Unified Strategy toward the Synthesis of Acerogenin-Type Macrocycles: Total Syntheses of Acerogenins A, B, C, and L and Aceroside IV | 3.5 | 60 | Citations (PDF) |
| 405 | Approach towards the total synthesis of cyclopeptide alkaloids | 1.4 | 19 | Citations (PDF) |
| 406 | Synthesis of cycloisodityrosine revisited: A selective ring forming process | 1.4 | 13 | Citations (PDF) |
| 407 | A method for removal of N-BOC protecting groups from substrates on TFA-sensitive resins | 1.4 | 58 | Citations (PDF) |
| 408 | Horse liver esterase catalyzed enantioselective hydrolysis of N,O-diacetyl-2-amino-1-arylethanol | 1.6 | 14 | Citations (PDF) |
| 409 | Asymmetric synthesis of 3,5-bis(isopropyloxy)-4-methoxyphenyl glycine by way of a diastereoselective Strecker reaction and an Evans electrophilic amination reaction | 1.6 | 16 | Citations (PDF) |
| 410 | An Efficient Chloro-deamination Procedure, Application to the Synthesis of Advanced Vancomycin C-O-D-O-E Ring | 1.4 | 11 | Citations (PDF) |
| 411 | First Total Synthesis of Acerogenin C and Aceroside IV | 3.5 | 39 | Citations (PDF) |
| 412 | A formal total synthesis of deoxybouvardin | 2.0 | 17 | Citations (PDF) |
| 413 | Chemoenzymatic synthesis of enantiomerically pure 4-fluoro-3-nitro and 3-fluoro-4-nitro phenylalanine | 1.6 | 33 | Citations (PDF) |
| 414 | In vitro and in vivo immunosuppressive potential of thalidomide and its derivative, N-hydroxythalidomide, alone and in combination with cyclosporin A | 1.3 | 11 | Citations (PDF) |
| 415 | 4-Nitrophenyltriflate as a new triflating agent | 1.4 | 38 | Citations (PDF) |
| 416 | Synthesis of four atropdiastereoisomers of C-O-D-O-E ring of vancomycin by sequential cycloetherifications | 1.4 | 19 | Citations (PDF) |
| 417 | A highly stereoselective synthesis of (2S, 3S)-β-hydroxyleucine | 1.4 | 24 | Citations (PDF) |
| 418 | Rapid and efficient solid phase syntheses of cyclic peptides with endocyclic biaryl ether bonds | 1.4 | 47 | Citations (PDF) |
| 419 | Solution phase combinatorial synthesis of arylpiperazines | 1.4 | 37 | Citations (PDF) |
| 420 | Synthesis of model tricyclic C-O-D-O-E-F-O-G ring of teicoplanin | 1.4 | 19 | Citations (PDF) |
| 421 | A Novel Strategy towards the Total Synthesis of Cyclopeptide Alkaloids | 1.4 | 0 | Citations (PDF) |
| 422 | Synthesis of Modified Carboxyl Binding Pockets of Vancomycin and Teicoplanin† | 3.5 | 59 | Citations (PDF) |
| 423 | Asymmetric Synthesis. 39.1Synthesis of 2-(1-Aminoalkyl)piperidinesvia2-Cyano-6-phenyl Oxazolopiperidine | 3.5 | 36 | Citations (PDF) |
| 424 | Selective Hydroxy Group Protection of Gallic Acid | 1.6 | 15 | Citations (PDF) |
| 425 | Synthesis of a model bicyclic C-O-D-O-E ring of vancomycin by a one-pot, double SNAr based macrocyclization | 3.4 | 31 | Citations (PDF) |
| 426 | Ein neuer Ansatz zur Totalsynthese von Cyclopeptid‐Alkaloiden | 1.4 | 12 | Citations (PDF) |
| 427 | A Novel Strategy towards the Total Synthesis of Cyclopeptide Alkaloids | 4.7 | 33 | Citations (PDF) |
| 428 | Synthesis of hapalosin and 8-deoxy-hapalosin | 1.4 | 31 | Citations (PDF) |
| 429 | A new access to 14-membered macrocycle: Synthesis of model F-O-G ring of teicoplanin | 1.4 | 35 | Citations (PDF) |
| 430 | Palladium catalyzed reductive deprotection of Alloc: Transprotection and peptide bond formation | 1.4 | 44 | Citations (PDF) |
| 431 | Asymmetric synthesis of (2S,3R) β-(4-F-3-NO2) phenyl serine, D-(R)-4-methoxy-3,5-bistbutyldimethylsiloxy phenylglycine and their assemblage to C-O-D ring of vancomycin | 1.4 | 48 | Citations (PDF) |
| 432 | The first synthesis of a model bicyclic D-O-E-F-O-G ring of teicoplanin via sequential intramolecular SNAr reactions | 1.4 | 22 | Citations (PDF) |
| 433 | Alkylation of Diethyl Acetamidomalonate by Weak Electrophiles | 1.6 | 5 | Citations (PDF) |
| 434 | A Convergent Synthesis of 14-Membered F-O-G Ring Analogs of the Teicoplanin Binding Pocket via Intramolecular SNAr Reaction | 3.5 | 50 | Citations (PDF) |
| 435 | Synthesis of A Modified Carboxylate-binding Pocket of Vancomycin | 1.4 | 30 | Citations (PDF) |
| 436 | Synthesis of a modified carboxylate-binding pocket of vancomycin | 1.4 | 10 | Citations (PDF) |
| 437 | Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4 | 1.4 | 99 | Citations (PDF) |
| 438 | An easy access to functionalized diaryl ethers: Formal total synthesis of K-13 | 1.4 | 29 | Citations (PDF) |
| 439 | A novel synthesis of K-13 | 1.4 | 42 | Citations (PDF) |
| 440 | The first examples of SNAr-based macrocyclisation: synthesis of model carboxylate-binding pockets of vancomycin | 1.9 | 20 | Citations (PDF) |
| 441 | SNAr-Based Macrocyclization: An Application to the Synthesis of Vancomycin Family Models | 3.5 | 93 | Citations (PDF) |
| 442 | A concise and efficient synthesis of protected actinoidic acid, the degradation product of vancomycin | 1.4 | 26 | Citations (PDF) |
| 443 | A SN Ar based facile synthesis of triaryl diethers, degradation products of vancomycin and related glycopeptide antibiotics | 1.4 | 18 | Citations (PDF) |
| 444 | Asymmetric synthesis. 29. Preparation of 1,8-diazaspiro[5.5]undecane derivatives | 3.5 | 31 | Citations (PDF) |
| 445 | Elemental white phosphorus as a radical trap: a new and general route to phosphonic acids | 15.0 | 77 | Citations (PDF) |
| 446 | An Efficient Procedure for the Regioselective Monoprotection of 1,2-Diols | 2.0 | 12 | Citations (PDF) |
| 447 | Asymmetric synthesis. XXXII. Formal synthesis of (-) - Perhydrohistrionicotoxin. | 1.4 | 22 | Citations (PDF) |
| 448 | Asymmetric synthesis XVIII | 1.4 | 30 | Citations (PDF) |
| 449 | Asymmetric synthesis xx preparation of a novel spiropiperidine system by the CN(R,S) method | 1.4 | 14 | Citations (PDF) |
| 450 | Copper‐Catalyzed Aza‐Sonogashira Cross‐Coupling To Form Ynimines: Development and Application to the Synthesis of Heterocycles | 1.4 | 2 | Citations (PDF) |
| 451 | Editing Tetrasubstituted Carbon: Dual C–O Bond Functionalization of Tertiary Alcohols Enabled by Palladium-Based Dyotropic Rearrangement | 15.0 | 8 | Citations (PDF) |
| 452 | Wacker Oxidation of Trisubstituted Alkenes: Pd(II)‐Catalyzed Oxidative Ring Expansion of Exocyclic <i>α,β</i>‐Unsaturated Carbonyl to 2‐Fluoro‐1,3‐Dicarbonyl Compounds | 1.4 | 0 | Citations (PDF) |
| 453 | Wacker Oxidation of Trisubstituted Alkenes: Pd(II)‐Catalyzed Oxidative Ring Expansion of Exocyclic <i>α,β</i>‐Unsaturated Carbonyl to 2‐Fluoro‐1,3‐Dicarbonyl Compounds | 14.4 | 4 | Citations (PDF) |
| 454 | Total Synthesis of (±)-Crokonoid A | 15.0 | 1 | Citations (PDF) |
| 455 | Concise Enantioselective Total Synthesis of (+)-Punctaporonin U | 15.0 | 1 | Citations (PDF) |
| 456 | Pd(II)/PIDA‐Enabled Migratory Triple Functionalization of Terminal Alkenes via a 1,2‐C/Pd(IV) Dyotropic Rearrangement | 1.4 | 0 | Citations (PDF) |
| 457 | Pd(II)/PIDA‐Enabled Migratory Triple Functionalization of Terminal Alkenes via a 1,2‐C/Pd(IV) Dyotropic Rearrangement | 14.4 | 2 | Citations (PDF) |
| 458 | Inherently chiral homo-heteracalixarenes: design and synthesis
<i>via</i>
an enantioselective intramolecular Sonogashira cross-coupling reaction | 7.1 | 1 | Citations (PDF) |
| 459 | Regio- and Enantioselective Pictet–Spengler Reaction of α-Diketones Catalyzed by a Single H-Bond Donor Organocatalyst | 12.4 | 1 | Citations (PDF) |
| 460 | Total Synthesis of (+)‐Melonine and (+)‐
N
4
‐Oxy Melonine Enabled by an Intramolecular Alkene Diamination Reaction | 1.4 | 0 | Citations (PDF) |
| 461 | Total Synthesis of (+)‐Melonine and (+)‐
N
4
‐Oxy Melonine Enabled by an Intramolecular Alkene Diamination Reaction | 14.4 | 0 | Citations (PDF) |
| 462 | Concerted 1,3-migration through regiodivergent consecutive 1,2-rearrangements using palladium catalysis | 18.1 | 0 | Citations (PDF) |
