Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
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Difluoromethanesulfonyl hypervalent iodonium ylides for electrophilic difluoromethylthiolation reactions under copper catalysisCopper-promoted sulfenylation of sp2 C-H bonds.Copper-Catalyzed Aerobic C-H Trifluoromethylation of Phenanthrolines.Recent advances in transition metal-catalyzed Csp(2)-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation.When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl HalidesIntroduction of fluorine and fluorine-containing functional groups.Silver-mediated trifluoromethoxylation of aryl stannanes and arylboronic acids.Silver-mediated trifluoromethylation of arenes using TMSCF3.Trifluoromethylthiolation of aryl iodides and bromides enabled by a bench-stable and easy-to-recover dinuclear palladium(i) catalyst.Efficient Synthesis of β-CF3/SCF3-Substituted Carbonyls via Copper-Catalyzed Electrophilic Ring-Opening Cross-Coupling of Cyclopropanols.Dual gold and photoredox catalysis: visible light-mediated intermolecular atom transfer thiosulfonylation of alkenes.Selective C-O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (ORF) arenes and heteroarenes.Sulfoxide-Directed Metal-Free ortho-Propargylation of Aromatics and Heteroaromatics.Nickel-catalyzed trifluoromethylthiolation of Csp2-O bonds.Base-catalyzed electrophilic trifluoromethylthiolation of terminal alkynes.Copper-boxmi complexes as highly enantioselective catalysts for electrophilic trifluoromethylthiolations.Copper(II)-catalyzed trifluoromethylation of N-aryl imines.Formation of C-SCF3 bonds through direct trifluoromethylthiolation.Generation of 4-((trifluoromethyl)thio)-2H-benzo[e][1,2]thiazine 1,1-dioxides via a reaction of trifluoromethanesulfanylamide with 2-(2-alkynyl)benzenesulfonamide.Copper-catalyzed trifluoromethyl thiolation--mild and efficient synthesis of trifluoromethyl thioethers.An efficient and practical approach to trifluoromethylthiolation of α-haloketones/α-haloarylmethanes.Oxidative nucleophilic strategy for synthesis of thiocyanates and trifluoromethyl sulfides from thiols.Tandem trifluoromethylthiolation/aryl migration of aryl alkynoates to trifluoromethylthiolated alkenes.Triphenylphosphine-Mediated Deoxygenative Reduction of CF3 SO2 Na and Its Application for Trifluoromethylthiolation of Aryl Iodides.Trifluoromethylthiolation and Trifluoromethylselenolation of α-Diazo Esters Catalyzed by Copper.Visible-Light-Promoted Trifluoromethylthiolation of Styrenes by Dual Photoredox/Halide Catalysis.Formation of α-SF5-Enolate Enables Preparation of 3-SF5-Quinolin-2-ones, 3-SF5-Quinolines, and 3-SF5-Pyridin-2-ones: Evaluation of their Physicochemical Properties.Trifluoromethyl Vinyl Sulfide: A Building Block for the Synthesis of CF3S-Containing Isoxazolidines.Elemental sulfur as a sulfuration agent in the copper-catalyzed C-H bond thiolation of electron-deficient arenes.Synthesis of difluoromethyl thioethers from difluoromethyl trimethylsilane and organothiocyanates generated in situ.Efficient silver-catalyzed direct sulfenylation and selenylation of rich arenes.Selenide-Catalyzed Stereoselective Construction of Tetrasubstituted Trifluoromethylthiolated Alkenes with Alkynes.Iodine-mediated regioselective synthesis of vinyl triflones from styrenes with CF3SO2Na.Chiral phosphoric acid-catalyzed asymmetric transfer hydrogenation of 3-trifluoromethylthioquinolines.Enantioselective Trifluoromethylthiolating Lactonization Catalyzed by an Indane-Based Chiral Sulfide.Regioselective ortho-trifluoromethylthiolation of 2-arylbenzo[d]thiazole via tandem substrate-assisted C-H iodination and trifluoromethylthiolation.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.Exploiting the unusual effects of fluorine in methodology.
P2860
Q28601782-33C4B85D-274D-49F5-A80D-4D5B9CA69717Q36399655-8C3893D7-8CD6-47F8-99B8-E7DF95409C34Q36549456-826C2792-38CD-434C-94B4-F0B129B4177EQ37406266-81713B9A-03EB-4E33-ADCD-9A1CF0A7F05DQ37684007-C8D7B29A-CCAF-4477-B15A-FF75C15DA3DCQ38123135-5E490893-3DB2-461D-9180-DAA39A937C30Q39172790-1E3BF0FA-0A72-41F5-89EC-EC451A058C78Q39547245-48CD466E-BD37-469A-8F15-ADBCCFF5E033Q41012429-2D03A841-F0B4-4DF9-A16D-4BACBDD3DA6EQ42173192-8FF2A95D-7248-4826-8F87-C62F2C851818Q42266895-4D98E461-7A98-4A09-86A9-D0104D2D7E50Q42284825-1724DF5F-7BE0-4C8D-8C98-9E4DC2955C07Q42414634-9CC07267-320B-41CE-A412-6DF53C424592Q42705550-3840FA70-763E-4043-8CEF-C966B6D3CB32Q43433859-8EDC00FA-9380-40A4-8461-5FD64390D166Q43589614-FE068967-7A3E-4B0A-974A-8A591DAC082DQ43677143-19323642-B5D4-46EA-8E21-6334A7D6393DQ43814306-741FA355-5900-43EE-B126-3A4AF8FEE23CQ45902607-A16C325B-73F5-4D80-AFE3-029BC8EA52CEQ46356243-2A8EF8F7-9002-4A5B-8B2E-AC63BDF3D038Q46719844-53DA1CCB-B941-4C89-AD04-67B45A34E44CQ46827834-0D94B9BB-8D7D-4115-B5DF-BB73E64289A0Q47745102-F09B0BDF-6397-4A5D-8694-11454A5876F5Q48094430-36E21C93-1C0C-46B5-9C14-F06AD93D25A1Q48174732-87F8BBA6-1884-4451-A818-00811D3A5336Q48237861-32A98641-8E7C-460C-9DA6-271BD9D10F27Q48269510-11194D55-8FBF-4F62-93D3-7AF28D335FA3Q48270905-9656D306-A2DF-482F-A13C-7E97199D0873Q49925140-EDB77D4D-F014-47C5-A459-85FB85529A59Q50999506-F0022D0C-FC73-4DF8-B5DE-C808E20B74ECQ51040969-0ABE1795-8CC7-49F8-B558-95A92F85F449Q51186109-2233E7C9-63E3-4164-A5B7-F381B842C718Q51194109-72642E1B-34C9-4054-9A35-682F79AB8694Q51278379-2274EEDD-184B-4E66-8F7B-F9C0CE12380DQ51407288-1363FE07-01D0-4D4B-8DBA-F2971426AE3CQ51528370-C5445A4B-A7E6-4551-A477-067462A6895CQ52874840-7449FDAE-E60E-4515-B5B9-58645F1E3E34Q53125556-54105E8F-6BA9-47A3-B1A7-47205475030BQ53293744-03F5227A-57D7-4AD5-BBB0-AD00D83E78E9Q53293752-11F1B2BC-B10B-4E8F-9DC3-86941FBBD5FD
P2860
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
@ast
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
@en
type
label
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
@ast
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
@en
prefLabel
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
@ast
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
@en
P2093
P2860
P356
P1476
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions.
@en
P2093
David S Surry
Georgiy Teverovskiy
Stephen L Buchwald
P2860
P304
P356
10.1002/ANIE.201102543
P407
P577
2011-06-20T00:00:00Z