Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
about
18F-Fluoroform: a 18F-trifluoromethylating agent for the synthesis of SCF218F-aromatic derivatives.Copper-promoted sulfenylation of sp2 C-H bonds.Recent advances in transition metal-catalyzed Csp(2)-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation.Organofluorine chemistry: Difluoromethylene motifs spaced 1,3 to each other imparts facial polarity to a cyclohexane ring.Late stage trifluoromethylthiolation strategies for organic compounds.Single enantiomer synthesis of α-(trifluoromethyl)-β-lactam.2-Diazo-1-phenyl-2-((trifluoromethyl)sulfonyl)ethan-1-one: Another Utility for Electrophilic Trifluoromethylthiolation Reactions.Sulfoxide-Directed Metal-Free ortho-Propargylation of Aromatics and Heteroaromatics.Base-catalyzed electrophilic trifluoromethylthiolation of terminal alkynes.Copper-boxmi complexes as highly enantioselective catalysts for electrophilic trifluoromethylthiolations.Copper-catalyzed trifluoromethyl thiolation--mild and efficient synthesis of trifluoromethyl thioethers.An efficient and practical approach to trifluoromethylthiolation of α-haloketones/α-haloarylmethanes.Triphenylphosphine-Mediated Deoxygenative Reduction of CF3 SO2 Na and Its Application for Trifluoromethylthiolation of Aryl Iodides.Direct Monofluoromethylthiolation with S-(Fluoromethyl) Benzenesulfonothioate.Trifluoromethylthiolation and Trifluoromethylselenolation of α-Diazo Esters Catalyzed by Copper.Visible-Light-Promoted Trifluoromethylthiolation of Styrenes by Dual Photoredox/Halide Catalysis.Transition metal-free direct trifluoromethylthiolation of indoles using trifluoromethanesulfonyl chloride in the presence of triphenylphosphine.Copper-catalyzed fluoroalkylation of alkynes, and alkynyl & vinyl carboxylic acids with fluoroalkyl halides.Direct Trifluoromethylthiolation and Perfluoroalkylthiolation of C(sp(2))-H Bonds with CF3SO2Na and RfSO2Na.Catalytic borylation of SCF₃-functionalized arenes by rhodium(I) boryl complexes: regioselective C-H activation at the ortho-position.Enantioselective electrophilic trifluoromethylthiolation of β-ketoesters: a case of reactivity and selectivity bias for organocatalysis.Cp*CoIII-catalyzed directed C-H trifluoromethylthiolation of 2-phenylpyridines and 6-arylpurines.Silver-mediated oxidative aliphatic C-H trifluoromethylthiolation.(18)F-Labeling of Aryl-SCF3, -OCF3 and -OCHF2 with [(18)F]Fluoride.Iron-mediated Markovnikov-selective hydro-trifluoromethylthiolation of unactivated alkenes.Synthesis of Cu(I) trifluoromethylselenates for trifluoromethylselenolation of aryl and alkyl halides.N-trifluoromethylthiophthalimide: a stable electrophilic SCF3 -reagent and its application in the catalytic asymmetric trifluoromethylsulfenylation.Transition-Metal-Free Trifluoromethylthiolation of N-HeteroarenesConformational analysis of 6-fluorosalicylic acidActivity of N,N′-dialkyl-2-trifluoromethylthioimidazolium salts as phase-transfer catalyst for the alkylation of active methylene compoundsHighlyortho-Selective Trifluoromethylthiolation Reactions using a Ligand Exchange Strategy
P2860
Q36369868-0EAAA4A9-A0FC-461E-91D9-F0FB17E3D1A3Q36399655-74DC0878-D26A-49ED-80B6-ECA68145C834Q37406266-6F1CE271-B77E-425B-BF9C-752C5949877CQ37587813-5A0BAFE1-1AF9-4C91-B741-FF9307A5A409Q38880232-FDD8795F-4766-47C3-9F4C-A407B6E1ED15Q42010991-38023C82-BA30-430E-90EA-884C3864961CQ42150661-ECAA3F3B-F3EA-463C-92F8-196D1EE32BFBQ42414634-3756C243-CF6B-4285-AC71-2BDDDC3AF658Q43433859-B927F88C-9955-451A-9334-24DB04FED86CQ43589614-F1A71D78-8703-4DA0-982A-51F2083EBAE9Q46356243-70B6B04F-1867-41FF-BC5E-9646EC13A935Q46719844-FD415F42-DB67-40D2-89BB-BE8E817F7275Q48094430-B72B5199-7FC9-4A98-800C-87D17E2FA4C8Q48157590-B8158778-8154-492C-835A-5B19E3E6C5DCQ48174732-9FDA4390-7097-431C-9DD7-FCCE25E79675Q48237861-A7982FB1-C053-4397-8508-251E964B1ECBQ48341079-A2A1ABDC-446B-429E-B5C1-8D4C38C99B08Q50882943-0C275AC1-B9B1-43AA-8E38-A99291447590Q51683221-76780589-F893-4937-8A2C-6E55DBEB8AB4Q52874840-07774473-D19D-4E35-8C06-3D97CB96F2B0Q53125556-6D09F505-0B95-4440-A624-BFAC9D30C284Q53293744-1CAD2FEF-809C-428C-9EA6-5F1799C7F090Q53305484-3B28C2AA-2C8B-4B8C-B33E-5C98A33A2BB0Q53441762-0F8A23BE-B231-470D-81E1-0448A75F62C8Q53667388-7F253AF1-0E36-437E-8D19-F9BD8DAC97FFQ54472538-7254E4DF-3F50-4E3F-91F3-DA49E9A575A5Q54765177-418831CE-9567-4FFC-B1BE-8C474FB9F0DEQ57657081-80729EAB-174E-487F-AAEE-ADB5FE321948Q57782723-B398E587-9250-4F22-9DC8-AAD6210D4169Q57795335-1B3E5EB5-844A-47E0-9E3E-460F539EC349Q58867274-A8270019-9550-4089-80CA-3D2F1DAC9045
P2860
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@ast
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@en
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@nl
type
label
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@ast
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@en
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@nl
prefLabel
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@ast
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@en
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@nl
P2860
P356
P1476
Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
@en
P2093
Vladimir N Boiko
P2860
P304
P356
10.3762/BJOC.6.88
P407
P577
2010-08-18T00:00:00Z