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Copper-Promoted Sulfenylation of sp 2 C–H Bonds

https://doi.org/10.1021/ja3092278
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Copper‐Catalyzed CC Bond Formation through CH Functionalization: Synthesis of Multisubstituted Indoles from N‐Aryl Enaminones
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Transition‐Metal‐Catalyzed Direct Arylation of (Hetero)Arenes by CH Bond Cleavage
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Pd‐Catalyzed Synthesis of ArSCF 3 Compounds under Mild Conditions
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Copper‐Catalyzed Aerobic Oxidative CH Functionalizations: Trends and Mechanistic Insights
inferredcites →https://doi.org/10.1002/anie.201108663openalex-snapshot
Copper‐Catalyzed Oxidative Trifluoromethylthiolation of Aryl Boronic Acids with TMSCF 3 and Elemental Sulfur
inferredcites →https://doi.org/10.1002/anie.201201491openalex-snapshot
Copper‐Mediated and Copper‐Catalyzed Cross‐Coupling of Indoles and 1,3‐Azoles: Double CH Activation
inferredcites →https://doi.org/10.1002/anie.201205156openalex-snapshot
Electrophilic Trifluoromethanesulfanylation of Organometallic Species with Trifluoromethanesulfanamides
inferredcites →https://doi.org/10.1002/asia.201200347openalex-snapshot
Oxidative Trifluoromethylthiolations of Aryl Boronic Acids Using a Copper/O 2 ‐Based Protocol
inferredcites →https://doi.org/10.1002/chem.200902374openalex-snapshot
Functionalization of Organic Molecules by Transition‐Metal‐Catalyzed C(sp 3 )H Activation
inferredcites →https://doi.org/10.1002/chin.201031153openalex-snapshot
ChemInform Abstract: Copper(II)‐Catalyzed ortho‐Acyloxylation of the 2‐Arylpyridines sp2 C—H Bonds with Anhydrides, Using O2 as Terminal Oxidant.
inferredcites →https://doi.org/10.1002/ejoc.200400702openalex-snapshot
Synthesis and Structural Characterization of Highly Fluorinated Sulfimides and Sulfoximides as Functional Building Blocks for Materials Science
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Recent Developments in Catalytic Aryl Coupling Reactions
inferredcites →https://doi.org/10.1002/ejoc.201000928openalex-snapshot
Transition‐Metal‐Catalyzed Direct C–H Alkenylation, Alkynylation, Benzylation, and Alkylation of (Hetero)arenes
inferredcites →https://doi.org/10.1002/ps.1829openalex-snapshot
The unique role of halogen substituents in the design of modern agrochemicals
inferredcites →https://doi.org/10.1016/j.jfluchem.2007.02.018openalex-snapshot
Selective oxidation and chlorination of trifluoromethylsulfide using trichloroisocyanuric acid in ionic liquid
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.09.009openalex-snapshot
New trends in the chemistry of α-fluorinated ethers, thioethers, amines and phosphines
inferredcites →https://doi.org/10.1016/j.tet.2008.10.053openalex-snapshot
Cu(II)-mediated oxidative dimerization of 2-phenylpyridine derivatives
inferredcites →https://doi.org/10.1016/s0022-1139(00)80106-2openalex-snapshot
Trifluoromethylthiocopper — stability and reaction chemistry
inferredcites →https://doi.org/10.1016/s0022-1139(02)00276-2openalex-snapshot
A new synthesis of trifluoromethanethiolates—characterization and properties of tetramethylammonium, cesium and di(benzo-15-crown-5)cesium trifluoromethanethiolates
inferredcites →https://doi.org/10.1016/s0022-1139(99)00063-9openalex-snapshot
Trifluoromethylthiolation of aromatic substrates using thiophosgene—fluoride salt reagents, and formation of byproducts with multi-carbon chains
inferredcites →https://doi.org/10.1016/s0022-1139(99)00157-8openalex-snapshot
Novel synthetic methodologies for fluorination and perfluoroalkylation
inferredcites →https://doi.org/10.1021/ar800164nopenalex-snapshot
Cross-Dehydrogenative Coupling (CDC): Exploring C−C Bond Formations beyond Functional Group Transformations
inferredcites →https://doi.org/10.1021/ar9000058openalex-snapshot
Palladium- and Copper-Catalyzed Arylation of Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/cr040075bopenalex-snapshot
α-Fluorinated Ethers, Thioethers, and Amines: Anomerically Biased Species
inferredcites →https://doi.org/10.1021/cr0509760openalex-snapshot
Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation
inferredcites →https://doi.org/10.1021/cr100280dopenalex-snapshot
Catalytic Dehydrogenative Cross-Coupling: Forming Carbon−Carbon Bonds by Oxidizing Two Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/cr900005nopenalex-snapshot
Rhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond Activation
inferredcites →https://doi.org/10.1021/cr900184eopenalex-snapshot
Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions
inferredcites →https://doi.org/10.1021/ic50062a038openalex-snapshot
Structure and properties of dibromo-N,N-dibutyldithiocarbamato complexes of copper(III) and gold(III)
inferredcites →https://doi.org/10.1021/ja01064a022openalex-snapshot
Reactions of Thiols with Sulfoxides. I. Scope of the Reaction and Synthetic Applications
inferredcites →https://doi.org/10.1021/ja054549fopenalex-snapshot
Highly Regioselective Arylation of sp 3 C−H Bonds Catalyzed by Palladium Acetate
inferredcites →https://doi.org/10.1021/ja061715qopenalex-snapshot
Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O 2 as an Oxidant
inferredcites →https://doi.org/10.1021/ja074669iopenalex-snapshot
Direct ortho Cupration: A New Route to Regioselectively Functionalized Aromatics
inferredcites →https://doi.org/10.1021/ja075802+openalex-snapshot
Copper-Catalyzed Arylation of Heterocycle C−H Bonds
inferredcites →https://doi.org/10.1021/ja1045378openalex-snapshot
Copper-Catalyzed Aerobic Oxidative Functionalization of an Arene C−H Bond: Evidence for an Aryl-Copper(III) Intermediate
inferredcites →https://doi.org/10.1021/ja1067993openalex-snapshot
A Direct Intramolecular C−H Amination Reaction Cocatalyzed by Copper(II) and Iron(III) as Part of an Efficient Route for the Synthesis of Pyrido[1,2-a]benzimidazoles fromN-Aryl-2-aminopyridines
inferredcites →https://doi.org/10.1021/ja111401hopenalex-snapshot
Copper-Mediated Intermolecular Direct Biaryl Coupling
inferredcites →https://doi.org/10.1021/ja2041942openalex-snapshot
Copper-Catalyzed Arylation of 1H-Perfluoroalkanes
inferredcites →https://doi.org/10.1021/ja2047717openalex-snapshot
A General Method for Copper-Catalyzed Arene Cross-Dimerization
inferredcites →https://doi.org/10.1021/ja210364ropenalex-snapshot
Nickel-Catalyzed Synthesis of Aryl Trifluoromethyl Sulfides at Room Temperature
inferredcites →https://doi.org/10.1021/ja210660gopenalex-snapshot
Highly Efficient Syntheses of Azetidines, Pyrrolidines, and Indolines via Palladium Catalyzed Intramolecular Amination of C(sp3)–H and C(sp2)–H Bonds at γ and δ Positions
inferredcites →https://doi.org/10.1021/ja210959popenalex-snapshot
Heterocycle Synthesis via Direct C–H/N–H Coupling
inferredcites →https://doi.org/10.1021/ja802123popenalex-snapshot
Carbon−Nitrogen Bond Formation Involving Well-Defined Aryl−Copper(III) Complexes
inferredcites →https://doi.org/10.1021/ja805688popenalex-snapshot
A General Method for Copper-Catalyzed Arylation of Arene C−H Bonds
inferredcites →https://doi.org/10.1021/ja907479jopenalex-snapshot
An Aromatic Glaser−Hay Reaction
inferredcites →https://doi.org/10.1021/ja910900popenalex-snapshot
Auxiliary-Assisted Palladium-Catalyzed Arylation and Alkylation of sp 2 and sp 3 Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/jm00269a003openalex-snapshot
Aromatic substituent constants for structure-activity correlations
inferredcites →https://doi.org/10.1021/jo030031nopenalex-snapshot
Chromium(VI) Oxide Catalyzed Oxidation of Sulfides to Sulfones with Periodic Acid
inferredcites →https://doi.org/10.1021/jo1000719openalex-snapshot
Copper(II)-Catalyzed Ortho-Acyloxylation of the 2-Arylpyridines sp2 C−H Bonds with Anhydrides, Using O2 as Terminal Oxidant
inferredcites →https://doi.org/10.1021/jo1014849openalex-snapshot
Copper-Catalyzed Thiolation of the Di- or Trimethoxybenzene Arene C−H Bond with Disulfides
inferredcites →https://doi.org/10.1021/jo2001808openalex-snapshot
Selective Sulfoxidation of Thioethers and Thioaryl Boranes with Nitrate, Promoted by a Molybdenum–Copper Catalytic System
inferredcites →https://doi.org/10.1021/jo200409hopenalex-snapshot
Copper-Catalyzed Amidation of 2-Phenylpyridine with Oxygen as the Terminal Oxidant
inferredcites →https://doi.org/10.1021/jo2017444openalex-snapshot
Copper-Mediated C–H Activation/C–S Cross-Coupling of Heterocycles with Thiols
inferredcites →https://doi.org/10.1021/jo202624sopenalex-snapshot
Lewis Acid-Catalyzed, Copper(II)-Mediated Synthesis of Heteroaryl Thioethers under Base-Free Conditions
inferredcites →https://doi.org/10.1021/jo900513zopenalex-snapshot
Copper-Catalyzed Synthesis of Benzoxazoles via a Regioselective C−H Functionalization/C−O Bond Formation under an Air Atmosphere
inferredcites →https://doi.org/10.1021/ol100449copenalex-snapshot
Cu(II)-Mediated Methylthiolation of Aryl C−H Bonds with DMSO
inferredcites →https://doi.org/10.1021/ol2000809openalex-snapshot
Copper(II)-Catalyzed Conversion of Bisaryloxime Ethers to 2-Arylbenzoxazoles via C−H Functionalization/C−N/C−O Bonds Formation
inferredcites →https://doi.org/10.1021/ol8013717openalex-snapshot
Copper-Mediated C−H Bond Arylation of Arenes with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ol902079gopenalex-snapshot
Copper-Mediated Amidation of Heterocyclic and Aromatic C−H Bonds
inferredcites →https://doi.org/10.1039/b606984nopenalex-snapshot
Direct transition metal-catalyzed functionalization of heteroaromatic compounds
inferredcites →https://doi.org/10.1039/b908581eopenalex-snapshot
Pd-catalyzed oxidative coupling with organometallic reagents via C–H activation
inferredcites →https://doi.org/10.1039/c0cc05557copenalex-snapshot
Copper(ii)-catalyzed ortho-functionalization of 2-arylpyridines with acyl chlorides
inferredcites →https://doi.org/10.1039/c39890001633openalex-snapshot
Synthesis and X-ray structure of bis(trifluoromethyl)(N,N-diethyldithiocarbamato)-copper; a remarkably stable perfluoroalkylcopper(III) complex
inferredcites →https://doi.org/10.1039/p19870002119openalex-snapshot
Trifluoromethanethiolate ion. Part 2. Nucleophilic substitution in pentafluoropyridine. Synthesis and characteristics of trifluoromethylthio and trifluoromethylsulphonyl derivatives
inferredcites →https://doi.org/10.1055/s-0029-1219061openalex-snapshot
An Aromatic Glaser-Hay Reaction
inferredcites →https://doi.org/10.1073/pnas.0601687103openalex-snapshot
Cu-catalyzed cross-dehydrogenative coupling: A versatile strategy for C–C bond formations via the oxidative activation of sp 3 C–H bonds
inferredcites →https://doi.org/10.1246/cl.2006.842openalex-snapshot
Amination of the Ortho C–H Bonds by the Cu(OAc)2-mediated Reaction of 2-Phenylpyridines with Anilines
inferredcites →https://doi.org/10.3762/bjoc.6.88openalex-snapshot
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Bis(trifluoromethyl)disulfide
inferred← citeshttps://doi.org/10.1002/047084289x.rn01830openalex-snapshot
8-Aminoquinoline
inferred← citeshttps://doi.org/10.1002/047084289x.rn01830.pub2openalex-snapshot
8‐Aminoquinoline
inferred← citeshttps://doi.org/10.1002/9781118690659.ch4openalex-snapshot
Alternative and Emerging Reagents for the Arylation of Heteronucleophiles
inferred← citeshttps://doi.org/10.1002/9781118754887.ch23openalex-snapshot
Chelate‐Assisted Arene C–H Bond Functionalization
inferred← citeshttps://doi.org/10.1002/9781119092490.ch11openalex-snapshot
Oxidation of Aryl sp2C─H Bond Assisted by Directing Group
inferred← citeshttps://doi.org/10.1002/9781119304197.ch13openalex-snapshot
Oxidative Couplings with C─H Bonds Forming C─P and C─S Bonds
inferred← citeshttps://doi.org/10.1002/9783527687800.ch7openalex-snapshot
Electrophilic Formation of Aromatic C–S Bonds
inferred← citeshttps://doi.org/10.1002/9783527697649.ch2openalex-snapshot
Ruthenium Catalysts for the Alkylation of Functionalized Arenes and Heteroaromatic Substrates via Hydroarylation
inferred← citeshttps://doi.org/10.1002/9783527699087.ch15openalex-snapshot
Organometallic Chelation‐Assisted C − H Functionalization
inferred← citeshttps://doi.org/10.1002/9783527824342.ch13openalex-snapshot
Trifluoromethylthiolation of Aromatic and Heteroaromatic Compounds
inferred← citeshttps://doi.org/10.1002/9783527825158.ch4openalex-snapshot
Introduction of Trifluoromethylthio Group into Organic Molecules
inferred← citeshttps://doi.org/10.1002/9783527826445.ch15openalex-snapshot
Copper‐Catalyzed C – H Activation
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0017openalex-snapshot
Pd‐Catalyzed CChalcogen Bond Formation (CS, CSe) by CH Bond Activation
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0056openalex-snapshot
Copper‐Catalyzed sp 2 CH Bond Functionalization
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0151openalex-snapshot
CH Functionalization Utilizing CO Surrogates
inferred← citeshttps://doi.org/10.1002/adsc.201400340openalex-snapshot
One‐Pot Sandmeyer Trifluoromethylation and Trifluoromethylthiolation
inferred← citeshttps://doi.org/10.1002/adsc.201400360openalex-snapshot
Thioesterification of Alkylbenzenes with Thiols via Copper‐ Catalyzed Cross‐Dehydrogenative Coupling without a Directing Group
inferred← citeshttps://doi.org/10.1002/adsc.201400362openalex-snapshot
Highly ortho‐Selective Trifluoromethylthiolation Reactions using a Ligand Exchange Strategy
inferred← citeshttps://doi.org/10.1002/adsc.201400561openalex-snapshot
Synthesis of Trifluoromethanesulfanylbenzofulvenes via a Cascade Electrophilic Cyclization under Mild Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201400717openalex-snapshot
Lewis Acid‐Catalyzed Electrophilic Trifluoromethylthiolation of (Hetero)Arenes
inferred← citeshttps://doi.org/10.1002/adsc.201400947openalex-snapshot
Copper‐Mediated ortho‐Nitration of Arene and Heteroarene CH Bonds Assisted by an 8‐Aminoquinoline Directing Group
inferred← citeshttps://doi.org/10.1002/adsc.201500575openalex-snapshot
Copper‐Mediated Trifluoromethylthiolation of Heteroaryl Bromides
inferred← citeshttps://doi.org/10.1002/adsc.201500606openalex-snapshot
Copper‐Catalyzed Trifluoromethylthiolation of Di(hetero)aryl‐λ3‐iodanes: Mechanistic Insight and Application to Synthesis of (Hetero)Aryl Trifluoromethyl Sulfides
inferred← citeshttps://doi.org/10.1002/adsc.201500791openalex-snapshot
Palladium‐Catalyzed CH Functionalization of Ferrocenecarboxylic Acid by using 8‐Aminoquinoline as a Removable Directing Group
inferred← citeshttps://doi.org/10.1002/adsc.201500884openalex-snapshot
Copper‐Mediated ortho ‐Arylation of Benzamides with Arylboronic Acid
inferred← citeshttps://doi.org/10.1002/adsc.201600031openalex-snapshot
Copper‐Catalyzed or ‐Mediated CH Bond Functionalizations Assisted by Bidentate Directing Groups
inferred← citeshttps://doi.org/10.1002/adsc.201600177openalex-snapshot
Nickel(II)‐Mediated Regioselective CH Monoiodination of Arenes and Heteroarenes by using Molecular Iodine
inferred← citeshttps://doi.org/10.1002/adsc.201600200openalex-snapshot
Disulfides as Sulfonylating Precursors for the Synthesis of Sulfone‐Containing Oxindoles
inferred← citeshttps://doi.org/10.1002/adsc.201600664openalex-snapshot
Directing Group‐Assisted Copper(II)‐Catalyzed ortho‐Carbonylation to Benzamide using 2,2′‐Azobisisobutyronitrile (AIBN)
inferred← citeshttps://doi.org/10.1002/adsc.201600775openalex-snapshot
Copper‐Mediated Tandem C( sp 2 )–H Sulfenylation and Annulation of Arenes with 2‐Mercaptoimidazoles: Regio‐ and Site‐selective Access to Polycyclic Fused Imidazo[2,1‐ b ][1,3]thiazinones
inferred← citeshttps://doi.org/10.1002/adsc.201600937openalex-snapshot
Late‐Stage Diversification of Non‐Steroidal Anti‐Inflammatory Drugs by Transition Metal‐Catalyzed C–H Alkenylations, Thiolations and Selenylations
inferred← citeshttps://doi.org/10.1002/adsc.201601298openalex-snapshot
Preparation of Electrophilic Trifluromethylthio Reagents from Nucleophilic Tetramethylammonium Trifluoromethylthiolate
inferred← citeshttps://doi.org/10.1002/adsc.201700066openalex-snapshot
(Pentamethylcyclopentadienyl)cobalt(III)‐Catalyzed Direct Trifluoromethylthiolation of Arenes via C−H Activation
inferred← citeshttps://doi.org/10.1002/adsc.201700270openalex-snapshot
Metal‐Free Difluoromethylthiolation, Trifluoromethylthiolation, and Perfluoroalkylthiolation with Sodium Difluoromethane‐ sulfinate, Sodium Trifluoromethanesulfinate or Sodium Perfluoro‐ alkanesulfinate
inferred← citeshttps://doi.org/10.1002/adsc.201700949openalex-snapshot
Copper‐Mediated Thiolation of Unactivated Heteroaryl C−H Bonds with Disulfides under Ligand‐ and Metal‐Oxidant‐Free Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201800090openalex-snapshot
Rhodium‐Catalyzed Direct and Selective ortho C−H Chalcogenation of N‐(Hetero)aryl‐7‐azaindoles
inferred← citeshttps://doi.org/10.1002/adsc.201800136openalex-snapshot
Synthesis of Monofluoromethylthioesters from Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.201800398openalex-snapshot
Cobalt‐Catalyzed Directed sp2 C−H Acetoxylation of Arenes Employing Mn(OAc)3 ⋅ 2H2O as Acetoxy Source
inferred← citeshttps://doi.org/10.1002/adsc.201800702openalex-snapshot
Tf2O‐Promoted Trifluoromethythiolation of Various Arenes Using NaSO2CF3
inferred← citeshttps://doi.org/10.1002/adsc.201800736openalex-snapshot
Visible Light‐Induced C−H Bond Functionalization: A Critical Review
inferred← citeshttps://doi.org/10.1002/adsc.201801138openalex-snapshot
Direct Oxidative Disulfenylation/Cyclization of 2′‐Hydroxyacetophenones with Thiophenols for the Synthesis of 2,2‐Dithio‐Benzofuran‐3(2 H )‐Ones
inferred← citeshttps://doi.org/10.1002/adsc.201900400openalex-snapshot
Iron‐Catalyzed Cross‐Dehydrogenative Coupling of Oxindoles with Thiols/Selenols for Direct C(sp3)−S/Se Bond Formation
inferred← citeshttps://doi.org/10.1002/adsc.201900643openalex-snapshot
Copper‐Catalyzed Domino Synthesis of Sulfur‐Containing Heterocycles Using Carbon Disulfide as a Building Block
inferred← citeshttps://doi.org/10.1002/adsc.201900864openalex-snapshot
Thiosulfonates as Emerging Reactants: Synthesis and Applications
inferred← citeshttps://doi.org/10.1002/adsc.201901316openalex-snapshot
Cu(II)‐Mediated C−C/C−O Bond Formation via C−H/C−C Bond Cleavage: Access to Benzofurans Using Amide as a Traceless Directing Group
inferred← citeshttps://doi.org/10.1002/adsc.202000112openalex-snapshot
Synthesis of Benzo[b]thiophenes through Rhodium‐Catalyzed Three‐Component Reaction using Elemental Sulfur
inferred← citeshttps://doi.org/10.1002/adsc.202000861openalex-snapshot
Deoxygenative 1,1‐Bis‐trifluoromethylthiolation of Aromatic Aldehydes to Access Bis(trifluoromethylthio)methylarenes
inferred← citeshttps://doi.org/10.1002/adsc.202200691openalex-snapshot
Palladium‐Catalyzed Remote δ‐C−H Selenylation of Arylethylamide and Alkenylethylamide Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.202300620openalex-snapshot
Copper‐Mediated C−H Chalcogenation of Heterocycles: Application to the Synthesis of Chalcogenoxanthones
inferred← citeshttps://doi.org/10.1002/adsc.202300719openalex-snapshot
Synthesis of Trifluoromethylthiolated Quinolinones via Trifluoromethanesulfanamide‐Induced Electrophilic Intramolecular Cyclization of N‐Arylpropynamides
inferred← citeshttps://doi.org/10.1002/ajoc.201402289openalex-snapshot
Copper‐Catalyzed Regioselective C5 Sulfenylation of Imidazo[2,1‐b]thiazoles with Thiols
inferred← citeshttps://doi.org/10.1002/ajoc.201500105openalex-snapshot
Reusable and Removable Directing Groups for C(sp2)−H Bond Functionalization of Arenes
inferred← citeshttps://doi.org/10.1002/ajoc.201600491openalex-snapshot
Selective Mono‐ and Di‐C(aryl)−H Sulfenylation of Benzamides by One‐Pot Assembly of 8‐Aminoquinoline, Benzoyl chlorides, and Thiophenols
inferred← citeshttps://doi.org/10.1002/ajoc.201700680openalex-snapshot
Iodine‐Catalyzed, Ethyl‐Lactate‐Mediated Synthesis of 1,4‐Benzothiazines via Metal‐Free Cascade Enaminone Transamination and C−H Sulfenylation
inferred← citeshttps://doi.org/10.1002/ajoc.201800276openalex-snapshot
Remote C−H Functionalization of 8‐Aminoquinolinamides
inferred← citeshttps://doi.org/10.1002/ajoc.201800351openalex-snapshot
Atom‐Economical and Stereoselective Difunctionalization of Electron‐Withdrawing Alkynes with N‐Trifluoromethylthiophthalimide
inferred← citeshttps://doi.org/10.1002/ajoc.201900199openalex-snapshot
Copper‐Mediated Direct and Selective C−H Thiolation of Quinazolinones
inferred← citeshttps://doi.org/10.1002/ajoc.201900358openalex-snapshot
Hydrogen‐Bonding‐Network‐Assisted Regioselective Trifluoromethylthiolation and Sulfenylation of Electron‐Rich (Hetero)arenes
inferred← citeshttps://doi.org/10.1002/ajoc.202000017openalex-snapshot
Rhodium‐Catalyzed Direct ortho C−H Thiolation of Cyclic N‐Sulfonyl Ketimines
inferred← citeshttps://doi.org/10.1002/ajoc.202000650openalex-snapshot
Electrolyte‐Triggered C5‐Selective Trifluoromethylation and Halogenation of 8‐Aminoquinoline Derivatives
inferred← citeshttps://doi.org/10.1002/ajoc.202100471openalex-snapshot
Selective Trifluoromethylthiolation of Unactivated C(sp3)−H Bonds Enabled by Excited Ketones
inferred← citeshttps://doi.org/10.1002/ajoc.202400588openalex-snapshot
Synthesis of Trifluoromethylthio Compounds from Sulfur‐Containing Precursors
inferred← citeshttps://doi.org/10.1002/ange.201206566openalex-snapshot
Einführung von Fluor und fluorhaltigen funktionellen Gruppen
inferred← citeshttps://doi.org/10.1002/ange.201209817openalex-snapshot
An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation
inferred← citeshttps://doi.org/10.1002/ange.201300135openalex-snapshot
Directed Amination of Non‐Acidic Arene CH Bonds by a Copper–Silver Catalytic System
inferred← citeshttps://doi.org/10.1002/ange.201300587openalex-snapshot
Copper‐Mediated CH/CH Biaryl Coupling of Benzoic Acid Derivatives and 1,3‐Azoles
inferred← citeshttps://doi.org/10.1002/ange.201301451openalex-snapshot
Katalytische Funktionalisierung von C(sp2)‐H‐ und C(sp3)‐H‐Bindungen unter Verwendung von zweizähnigen dirigierenden Gruppen
inferred← citeshttps://doi.org/10.1002/ange.201301891openalex-snapshot
Copper‐Catalyzed Regioselective Fluorination of Allylic Halides
inferred← citeshttps://doi.org/10.1002/ange.201303556openalex-snapshot
8‐Aminochinolin: eine wirkungsvolle dirigierende Gruppe in der metallkatalysierten direkten Funktionalisierung von C‐H‐Bindungen
inferred← citeshttps://doi.org/10.1002/ange.201304957openalex-snapshot
N‐Trifluormethylthiophthalimid: ein stabiles, elektrophiles SCF3‐ Reagens und seine Anwendung in der katalytischen asymmetrischen Trifluormethylsulfenylierung
inferred← citeshttps://doi.org/10.1002/ange.201305075openalex-snapshot
Enantioselective Electrophilic Trifluoromethylthiolation of β‐Ketoesters: A Case of Reactivity and Selectivity Bias for Organocatalysis
inferred← citeshttps://doi.org/10.1002/ange.201305179openalex-snapshot
Base‐Catalyzed Electrophilic Trifluoromethylthiolation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/ange.201305615openalex-snapshot
Use of a Readily Removable Auxiliary Group for the Synthesis of Pyrrolidones by the Palladium‐Catalyzed Intramolecular Amination of Unactivated γ C(sp3)H Bonds
inferred← citeshttps://doi.org/10.1002/ange.201307484openalex-snapshot
Direct Catalytic Trifluoromethylthiolation of Boronic Acids and Alkynes Employing Electrophilic Shelf‐Stable N‐(trifluoromethylthio)phthalimide
inferred← citeshttps://doi.org/10.1002/ange.201309584openalex-snapshot
Nickel‐katalysierte C‐H‐Alkylierung: direkte sekundäre Alkylierung und Trifluorethylierung von Arenen
inferred← citeshttps://doi.org/10.1002/ange.201310897openalex-snapshot
Structural Reevaluation of the Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation Supported by the Crystalline Sponge Method for X‐ray Analysis
inferred← citeshttps://doi.org/10.1002/ange.201311024openalex-snapshot
Eisen‐katalysierte C(sp2)‐H‐ und C(sp3)‐H‐Arylierung mit Triazol‐Unterstützung
inferred← citeshttps://doi.org/10.1002/ange.201311263openalex-snapshot
Copper‐Catalyzed Site‐Selective Intramolecular Amidation of Unactivated C(sp3)H Bonds
inferred← citeshttps://doi.org/10.1002/ange.201403983openalex-snapshot
N‐Trifluoromethylthiosaccharin: An Easily Accessible, Shelf‐Stable, Broadly Applicable Trifluoromethylthiolating Reagent
inferred← citeshttps://doi.org/10.1002/ange.201404579openalex-snapshot
Cobalt‐Catalyzed, Aminoquinoline‐Directed C(sp2)H Bond Alkenylation by Alkynes
inferred← citeshttps://doi.org/10.1002/ange.201406228openalex-snapshot
Copper‐Mediated C6‐Selective Dehydrogenative Heteroarylation of 2‐Pyridones with 1,3‐Azoles
inferred← citeshttps://doi.org/10.1002/ange.201406424openalex-snapshot
Catalytic Borylation of SCF3‐Functionalized Arenes by Rhodium(I) Boryl Complexes: Regioselective CH Activation at the ortho‐Position
inferred← citeshttps://doi.org/10.1002/ange.201409983openalex-snapshot
Direct Dehydroxytrifluoromethylthiolation of Alcohols Using Silver(I) Trifluoromethanethiolate and Tetra‐n‐butylammonium Iodide
inferred← citeshttps://doi.org/10.1002/ange.201411807openalex-snapshot
Silver‐Mediated Oxidative Aliphatic CH Trifluoromethylthiolation
inferred← citeshttps://doi.org/10.1002/ange.201411953openalex-snapshot
Direct Trifluoromethylthiolation of Unactivated C(sp3)H Using Silver(I) Trifluoromethanethiolate and Potassium Persulfate
inferred← citeshttps://doi.org/10.1002/ange.201500899openalex-snapshot
Synthesis of Difluoromethyl Thioethers from Difluoromethyl Trimethylsilane and Organothiocyanates Generated In Situ
inferred← citeshttps://doi.org/10.1002/ange.201502666openalex-snapshot
Regioselective Nucleophilic Functionalization of Antiaromatic Nickel(II) Norcorroles
inferred← citeshttps://doi.org/10.1002/ange.201508495openalex-snapshot
Direct Trifluoromethylthiolation and Perfluoroalkylthiolation of C(sp2)H Bonds with CF3SO2Na and RfSO2Na
inferred← citeshttps://doi.org/10.1002/ange.201600649openalex-snapshot
Ruthenium‐Catalyzed Hydroarylation and One‐Pot Twofold Unsymmetrical C−H Functionalization of Arenes
inferred← citeshttps://doi.org/10.1002/ange.201608011openalex-snapshot
New Design of a Disulfurating Reagent: Facile and Straightforward Pathway to Unsymmetrical Disulfanes by Copper‐Catalyzed Oxidative Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/ange.201609574openalex-snapshot
Superacid‐Catalyzed Trifluoromethylthiolation of Aromatic Amines
inferred← citeshttps://doi.org/10.1002/ange.201703841openalex-snapshot
Catalytic Oxidative Trifluoromethoxylation of Allylic C−H Bonds Using a Palladium Catalyst
inferred← citeshttps://doi.org/10.1002/ange.201805927openalex-snapshot
Synergistic Catalysis for the Umpolung Trifluoromethylthiolation of Tertiary Ethers
inferred← citeshttps://doi.org/10.1002/ange.201903511openalex-snapshot
Ligand‐Promoted RhIII‐Catalyzed Thiolation of Benzamides with a Broad Disulfide Scope
inferred← citeshttps://doi.org/10.1002/ange.202400308openalex-snapshot
Enantioselective Construction of C−SCF3 Stereocenters via Nickel Catalyzed Asymmetric Negishi Coupling Reaction
inferred← citeshttps://doi.org/10.1002/ange.202411870openalex-snapshot
Hemilabile and Redox‐Active Quinone Ligands Unlock sp3‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation
inferred← citeshttps://doi.org/10.1002/ange.8768278openalex-snapshot
Copper‐Catalyzed Enantioselective C–H Phosphorylation Enabled by a 3,3’‐Difluorinated BINOL Ligand
inferred← citeshttps://doi.org/10.1002/anie.201206566openalex-snapshot
Introduction of Fluorine and Fluorine‐Containing Functional Groups
inferred← citeshttps://doi.org/10.1002/anie.201209817openalex-snapshot
An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation
inferred← citeshttps://doi.org/10.1002/anie.201300135openalex-snapshot
Directed Amination of Non‐Acidic Arene CH Bonds by a Copper–Silver Catalytic System
inferred← citeshttps://doi.org/10.1002/anie.201300587openalex-snapshot
Copper‐Mediated CH/CH Biaryl Coupling of Benzoic Acid Derivatives and 1,3‐Azoles
inferred← citeshttps://doi.org/10.1002/anie.201301451openalex-snapshot
Catalytic Functionalization of C(sp 2 )H and C(sp 3 )H Bonds by Using Bidentate Directing Groups
inferred← citeshttps://doi.org/10.1002/anie.201301891openalex-snapshot
Copper‐Catalyzed Regioselective Fluorination of Allylic Halides
inferred← citeshttps://doi.org/10.1002/anie.201303556openalex-snapshot
8‐Aminoquinoline: A Powerful Directing Group in Metal‐Catalyzed Direct Functionalization of CH Bonds
inferred← citeshttps://doi.org/10.1002/anie.201304957openalex-snapshot
N‐Trifluoromethylthiophthalimide: A Stable Electrophilic SCF3‐Reagent and its Application in the Catalytic Asymmetric Trifluoromethylsulfenylation
inferred← citeshttps://doi.org/10.1002/anie.201305075openalex-snapshot
Enantioselective Electrophilic Trifluoromethylthiolation of β‐Ketoesters: A Case of Reactivity and Selectivity Bias for Organocatalysis
inferred← citeshttps://doi.org/10.1002/anie.201305179openalex-snapshot
Base‐Catalyzed Electrophilic Trifluoromethylthiolation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/anie.201305615openalex-snapshot
Use of a Readily Removable Auxiliary Group for the Synthesis of Pyrrolidones by the Palladium‐Catalyzed Intramolecular Amination of Unactivated γ C(sp3)H Bonds
inferred← citeshttps://doi.org/10.1002/anie.201307484openalex-snapshot
Direct Catalytic Trifluoromethylthiolation of Boronic Acids and Alkynes Employing Electrophilic Shelf‐Stable N‐(trifluoromethylthio)phthalimide
inferred← citeshttps://doi.org/10.1002/anie.201309584openalex-snapshot
Nickel‐Catalyzed CH Alkylations: Direct Secondary Alkylations and Trifluoroethylations of Arenes
inferred← citeshttps://doi.org/10.1002/anie.201310897openalex-snapshot
Structural Reevaluation of the Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation Supported by the Crystalline Sponge Method for X‐ray Analysis
inferred← citeshttps://doi.org/10.1002/anie.201311024openalex-snapshot
Iron‐Catalyzed C(sp2)H and C(sp3)H Arylation by Triazole Assistance
inferred← citeshttps://doi.org/10.1002/anie.201311263openalex-snapshot
Copper‐Catalyzed Site‐Selective Intramolecular Amidation of Unactivated C(sp 3 )H Bonds
inferred← citeshttps://doi.org/10.1002/anie.201403983openalex-snapshot
N ‐Trifluoromethylthiosaccharin: An Easily Accessible, Shelf‐Stable, Broadly Applicable Trifluoromethylthiolating Reagent
inferred← citeshttps://doi.org/10.1002/anie.201404579openalex-snapshot
Cobalt‐Catalyzed, Aminoquinoline‐Directed C(sp 2 )H Bond Alkenylation by Alkynes
inferred← citeshttps://doi.org/10.1002/anie.201406228openalex-snapshot
Copper‐Mediated C6‐Selective Dehydrogenative Heteroarylation of 2‐Pyridones with 1,3‐Azoles
inferred← citeshttps://doi.org/10.1002/anie.201406424openalex-snapshot
Catalytic Borylation of SCF3‐Functionalized Arenes by Rhodium(I) Boryl Complexes: Regioselective CH Activation at the ortho‐Position
inferred← citeshttps://doi.org/10.1002/anie.201409983openalex-snapshot
Direct Dehydroxytrifluoromethylthiolation of Alcohols Using Silver(I) Trifluoromethanethiolate and Tetra‐n‐butylammonium Iodide
inferred← citeshttps://doi.org/10.1002/anie.201411807openalex-snapshot
Silver‐Mediated Oxidative Aliphatic CH Trifluoromethylthiolation
inferred← citeshttps://doi.org/10.1002/anie.201411953openalex-snapshot
Direct Trifluoromethylthiolation of Unactivated C(sp 3 )H Using Silver(I) Trifluoromethanethiolate and Potassium Persulfate
inferred← citeshttps://doi.org/10.1002/anie.201500899openalex-snapshot
Synthesis of Difluoromethyl Thioethers from Difluoromethyl Trimethylsilane and Organothiocyanates Generated In Situ
inferred← citeshttps://doi.org/10.1002/anie.201502666openalex-snapshot
Regioselective Nucleophilic Functionalization of Antiaromatic Nickel(II) Norcorroles
inferred← citeshttps://doi.org/10.1002/anie.201508495openalex-snapshot
Direct Trifluoromethylthiolation and Perfluoroalkylthiolation of C(sp2)H Bonds with CF3SO2Na and RfSO2Na
inferred← citeshttps://doi.org/10.1002/anie.201600649openalex-snapshot
Ruthenium‐Catalyzed Hydroarylation and One‐Pot Twofold Unsymmetrical C−H Functionalization of Arenes
inferred← citeshttps://doi.org/10.1002/anie.201608011openalex-snapshot
New Design of a Disulfurating Reagent: Facile and Straightforward Pathway to Unsymmetrical Disulfanes by Copper‐Catalyzed Oxidative Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/anie.201609574openalex-snapshot
Superacid‐Catalyzed Trifluoromethylthiolation of Aromatic Amines
inferred← citeshttps://doi.org/10.1002/anie.201703841openalex-snapshot
Catalytic Oxidative Trifluoromethoxylation of Allylic C−H Bonds Using a Palladium Catalyst
inferred← citeshttps://doi.org/10.1002/anie.201805927openalex-snapshot
Synergistic Catalysis for the Umpolung Trifluoromethylthiolation of Tertiary Ethers
inferred← citeshttps://doi.org/10.1002/anie.201903511openalex-snapshot
Ligand‐Promoted RhIII‐Catalyzed Thiolation of Benzamides with a Broad Disulfide Scope
inferred← citeshttps://doi.org/10.1002/anie.202400308openalex-snapshot
Enantioselective Construction of C−SCF3 Stereocenters via Nickel Catalyzed Asymmetric Negishi Coupling Reaction
inferred← citeshttps://doi.org/10.1002/anie.202411870openalex-snapshot
Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation
inferred← citeshttps://doi.org/10.1002/anie.8768278openalex-snapshot
Copper‐Catalyzed Enantioselective C–H Phosphorylation Enabled by a 3,3’‐Difluorinated BINOL Ligand
inferred← citeshttps://doi.org/10.1002/asia.201300636openalex-snapshot
Transfer of Sulfur: From Simple to Diverse
inferred← citeshttps://doi.org/10.1002/asia.201402510openalex-snapshot
Copper‐Promoted Site‐Selective Acyloxylation of Unactivated C(sp3)H Bonds
inferred← citeshttps://doi.org/10.1002/asia.201901334openalex-snapshot
8‐Aminoquinoline‐Assisted Synthesis and Crystal Structure Studies of Ferrocenyl Aryl Sulfones
inferred← citeshttps://doi.org/10.1002/bkcs.70031openalex-snapshot
Cp * Co ( III )‐catalyzed C – H functionalization of bioactive heterocyclic motifs
inferred← citeshttps://doi.org/10.1002/cctc.201500673openalex-snapshot
Regioselective C−S Bond Formation between Flavones and Arylsulfonyl Chlorides through the Use of Ammonium Iodide
inferred← citeshttps://doi.org/10.1002/cctc.201600039openalex-snapshot
Tunable Di‐ and Mono‐γ‐C−H Arylation of Phenylacetamides by Palladium‐Catalyzed Domino Reactions
inferred← citeshttps://doi.org/10.1002/cctc.201701596openalex-snapshot
Coordinating Activation Strategy‐Induced Selective C−H Trifluoromethylation of Anilines
inferred← citeshttps://doi.org/10.1002/ceur.202500209openalex-snapshot
Synthesis of Cyclic Sulfilimines and Sulfoximines via Copper‐Mediated C(sp 2 )–H Sulfanylation of Benzylamines with a Catalytic Transient Directing Group
inferred← citeshttps://doi.org/10.1002/chem.201302692openalex-snapshot
Copper‐Catalyzed Trifluoromethyl Thiolation—Mild and Efficient Synthesis of Trifluoromethyl Thioethers
inferred← citeshttps://doi.org/10.1002/chem.201303459openalex-snapshot
[1,4]‐S‐ to O‐Silyl Migration: Multicomponent Synthesis of α‐Thioketones through Chemoselective Transformation of Esters to Ketones with Organolithium Reagents
inferred← citeshttps://doi.org/10.1002/chem.201303641openalex-snapshot
Copper–Boxmi Complexes as Highly Enantioselective Catalysts for Electrophilic Trifluoromethylthiolations
inferred← citeshttps://doi.org/10.1002/chem.201303730openalex-snapshot
Rhodium‐Catalyzed Directed Sulfenylation of Arene CH Bonds
inferred← citeshttps://doi.org/10.1002/chem.201303934openalex-snapshot
Synthesis of CuI Trifluoromethylselenates for Trifluoromethylselenolation of Aryl and Alkyl Halides
inferred← citeshttps://doi.org/10.1002/chem.201304717openalex-snapshot
Palladium‐Catalyzed Direct Thiolation of Aryl CH Bonds with Disulfides
inferred← citeshttps://doi.org/10.1002/chem.201402679openalex-snapshot
Direct Trifluoromethylthiolation of Alcohols under Mild Reaction Conditions: Conversion of ROH into RSCF3
inferred← citeshttps://doi.org/10.1002/chem.201402815openalex-snapshot
Copper‐Catalyzed Aerobic Oxidative NS Bond Functionalization for CS Bond Formation: Regio‐ and Stereoselective Synthesis of Sulfones and Thioethers
inferred← citeshttps://doi.org/10.1002/chem.201403019openalex-snapshot
Triazole‐Assisted Ruthenium‐Catalyzed CH Arylation of Aromatic Amides
inferred← citeshttps://doi.org/10.1002/chem.201403363openalex-snapshot
Copper‐Mediated ortho‐Nitration of (Hetero)Arenecarboxylates
inferred← citeshttps://doi.org/10.1002/chem.201404000openalex-snapshot
Copper‐Catalyzed Mild Nitration of Protected Anilines
inferred← citeshttps://doi.org/10.1002/chem.201404537openalex-snapshot
Recent Progress in Direct Introduction of Fluorinated Groups on Alkenes and Alkynes by means of CH Bond Functionalization
inferred← citeshttps://doi.org/10.1002/chem.201405594openalex-snapshot
Copper/Silver‐Mediated Direct ortho‐Ethynylation of Unactivated (Hetero)aryl CH Bonds with Terminal Alkyne
inferred← citeshttps://doi.org/10.1002/chem.201500957openalex-snapshot
Transition‐Metal‐Free Trifluoromethylthiolation of N‐Heteroarenes
inferred← citeshttps://doi.org/10.1002/chem.201502338openalex-snapshot
Mild and Soft Catalyzed Trifluoromethylthiolation of Boronic Acids: The Crucial Role of Water
inferred← citeshttps://doi.org/10.1002/chem.201502914openalex-snapshot
Synthesis of Aryl Tri‐ and Difluoromethyl Thioethers via a CH‐Thiocyanation/Fluoroalkylation Cascade
inferred← citeshttps://doi.org/10.1002/chem.201503524openalex-snapshot
Sandmeyer‐Type Trifluoromethylthiolation and Trifluoromethylselenolation of (Hetero)Aromatic Amines Catalyzed by Copper
inferred← citeshttps://doi.org/10.1002/chem.201503915openalex-snapshot
Iron‐Catalyzed Decarboxylation of Trifluoroacetate and Its Application to the Synthesis of Trifluoromethyl Thioethers
inferred← citeshttps://doi.org/10.1002/chem.201504790openalex-snapshot
Triphenylphosphine‐Mediated Deoxygenative Reduction of CF3SO2Na and Its Application for Trifluoromethylthiolation of Aryl Iodides
inferred← citeshttps://doi.org/10.1002/chem.201600190openalex-snapshot
Visible‐Light‐Promoted Trifluoromethylthiolation of Styrenes by Dual Photoredox/Halide Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201600229openalex-snapshot
Photocatalytic/Cu‐Promoted C−H Activations: Visible‐light‐Induced ortho‐Selective Perfluoroalkylation of Benzamides
inferred← citeshttps://doi.org/10.1002/chem.201601821openalex-snapshot
Weak O‐Assistance Outcompeting Strong N,N‐Bidentate Directing Groups in Copper‐Catalyzed C−H Chalcogenation
inferred← citeshttps://doi.org/10.1002/chem.201602730openalex-snapshot
Trifluoromethylthiolation and Trifluoromethylselenolation of α‐Diazo Esters Catalyzed by Copper
inferred← citeshttps://doi.org/10.1002/chem.201602909openalex-snapshot
Stereoretentive Copper‐Catalyzed Directed Thioglycosylation of C(sp 2 )−H Bonds of Benzamides
inferred← citeshttps://doi.org/10.1002/chem.201603092openalex-snapshot
Nickel‐Catalyzed C−H Chalcogenation of Anilines
inferred← citeshttps://doi.org/10.1002/chem.201604344openalex-snapshot
Bridging C−H Activation: Mild and Versatile Cleavage of the 8‐Aminoquinoline Directing Group
inferred← citeshttps://doi.org/10.1002/chem.201805938openalex-snapshot
Mo‐Based Oxidizers as Powerful Tools for the Synthesis of Thia‐ and Selenaheterocycles
inferred← citeshttps://doi.org/10.1002/chem.202003521openalex-snapshot
Pd‐Catalyzed Directed Thiocyanation Reaction by C−H Bond Activation
inferred← citeshttps://doi.org/10.1002/chem.202100093openalex-snapshot
A Guide to Directing Group Removal: 8‐Aminoquinoline
inferred← citeshttps://doi.org/10.1002/chem.202102121openalex-snapshot
Aromatic Trifluoromethylselenolation via Pd‐catalyzed C−H functionalization
inferred← citeshttps://doi.org/10.1002/chem.202202099openalex-snapshot
Directed Palladium Catalyzed C−H (Ethoxycarbonyl)difluoromethylthiolation Reactions
inferred← citeshttps://doi.org/10.1002/cjoc.201300415openalex-snapshot
Nucleophilic Trifluoromethylthiolation of Allylic Bromides: A Facile Preparation of Allylic Trifluoromethyl Thioethers
inferred← citeshttps://doi.org/10.1002/cjoc.201400392openalex-snapshot
Chincona Alkaloid‐Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles
inferred← citeshttps://doi.org/10.1002/cjoc.201500890openalex-snapshot
State‐of‐the‐Art in Electrophilic Trifluoromethylthiolation Reagents
inferred← citeshttps://doi.org/10.1002/cjoc.201600052openalex-snapshot
A Convenient Process for the Preparation of Heteroaryl Trifluoromethyl Selenoethers
inferred← citeshttps://doi.org/10.1002/cjoc.201600826openalex-snapshot
Direct Triflylation of Benzylic C—H Bonds with Pyridine as a Directing Group
inferred← citeshttps://doi.org/10.1002/cjoc.201700289openalex-snapshot
Regioselective Synthesis of SCF3‐Substituted 2,4‐Diarylquinazoline Using AgSCF3 as Trifluoromethylthiolation Reagent
inferred← citeshttps://doi.org/10.1002/cjoc.201800334openalex-snapshot
Copper‐Mediated Cyanation of Aryl C—H Bond with Removable Bidenate Auxiliary Using Acetonitrile as the Cyano Source
inferred← citeshttps://doi.org/10.1002/cjoc.201900090openalex-snapshot
From Reactivity and Regioselectivity to Stereoselectivity: An Odyssey of Designing PIP Amine and Related Directing Groups for C—H Activation
inferred← citeshttps://doi.org/10.1002/cmdc.201400059openalex-snapshot
Bis(pentafluorosulfanyl)phenyl Azide as an Expeditious Tool for Click Chemistry toward Antitumor Pharmaceuticals
inferred← citeshttps://doi.org/10.1002/ejoc.201301857openalex-snapshot
Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept
inferred← citeshttps://doi.org/10.1002/ejoc.201402105openalex-snapshot
Trifluoromethylthiolation of Diazo Compounds through Copper Carbene Migratory Insertion
inferred← citeshttps://doi.org/10.1002/ejoc.201402480openalex-snapshot
Synthesis of Allylic and Propargylic Trifluoromethyl Thioethers by Copper(I)‐Catalyzed Trifluoromethylthiolation of Allylic Bromides and Propargylic Chlorides
inferred← citeshttps://doi.org/10.1002/ejoc.201402533openalex-snapshot
Oxidative Trifluoromethylthiolation of Terminal Alkynes with AgSCF3: A Convenient Approach to Alkynyl Trifluoromethyl Sulfides
inferred← citeshttps://doi.org/10.1002/ejoc.201402629openalex-snapshot
(Trifluoromethyl)thiolation of 2‐Alkynylbenzoates: An Efficient Route to 4‐[(Trifluoromethyl)thio]‐1 H ‐isochromen‐1‐ones
inferred← citeshttps://doi.org/10.1002/ejoc.201500222openalex-snapshot
One‐Pot Synthesis of N‐Aryl‐Nicotinamides and Diarylamines Based on a Tunable Smiles Rearrangement
inferred← citeshttps://doi.org/10.1002/ejoc.201500384openalex-snapshot
Copper(I)‐Mediated Direct Trifluoromethylthiolation of Allylic Halides with Elemental Sulfur and (Trifluoromethyl)trimethylsilane
inferred← citeshttps://doi.org/10.1002/ejoc.201501148openalex-snapshot
Regioselective Mono‐ and Bis‐Sulfenylation of Active Methylene Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.201501623openalex-snapshot
Trifluoromethylthiolation of Unsymmetrical λ3‐Iodane Derivatives: Additive‐Free, Selective and Scalable Introduction of the SCF3 Group
inferred← citeshttps://doi.org/10.1002/ejoc.201600588openalex-snapshot
Palladium‐Catalyzed C–S Bond Formation of Stable Enamines with Arene/Alkanethiols: Highly Regioselective Synthesis of β‐Amino Sulfides
inferred← citeshttps://doi.org/10.1002/ejoc.201601253openalex-snapshot
Emergence of Unactivated Olefins for the Synthesis of Olefinated Arenes
inferred← citeshttps://doi.org/10.1002/ejoc.201601613openalex-snapshot
Methylsulfenylation of Electrophilic Carbon Atoms: Reaction Development, Scope, and Mechanism
inferred← citeshttps://doi.org/10.1002/ejoc.201700147openalex-snapshot
Copper‐Promoted Thiolation of C(sp2)–H Bonds Using a 2‐Amino Alkylbenzimidazole Directing Group
inferred← citeshttps://doi.org/10.1002/ejoc.201701339openalex-snapshot
Radical Aromatic Trifluoromethylthiolation: Photoredox Catalysis vs. Base Mediation
inferred← citeshttps://doi.org/10.1002/ejoc.201800418openalex-snapshot
Trifluoromethylthiolation of α‐Chloroaldehydes: Access to Quaternary SCF3‐Containing Centers
inferred← citeshttps://doi.org/10.1002/ejoc.201800451openalex-snapshot
Palladium‐Catalyzed Trifluoromethylthiolation of Chelation‐Assisted C–H Bonds
inferred← citeshttps://doi.org/10.1002/ejoc.201800790openalex-snapshot
Metal‐Catalyzed C–H Functionalization Processes with “Click”‐Triazole Assistance
inferred← citeshttps://doi.org/10.1002/ejoc.201801071openalex-snapshot
Pd‐Catalyzed Trifluoromethylthiolation of Unsaturated Compounds: A General Approach
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