Room temperature nucleophilic trifluoromethylthiolation of benzyl bromides with (bpy)Cu(SCF3)

Tetrahedron

Volumn 69, Issue 30, 2013, Pages 6046-6050

  Kong, Dedao ^a   Jiang, Zhou ^a   Xin, Shaogang ^a   Bai, Zhengshuai ^a   Yuan, Yaofeng ^a   Weng, Zhiqiang ^a  

^a FUZHOU UNIVERSITY   (China)

Author keywords

Benzyl bromides; Copper reagent; Trifluoromethylthiolation

Indexed keywords

(2 NITROBENZYL)(TRIFLUOROMETHYL)SULFANE; (3 CHLOROBENZYL)(TRIFLUOROMETHYL)SULFANE; (3 FLUOROBENZYL)(TRIFLUOROMETHYL)SULFANE; (3 METHOXYBENZYL)(TRIFLUOROMETHYL)SULFANE; (3 METHYLBENZYL)(TRIFLUOROMETHYL)SULFANE; (3 NITROBENZYL)(TRIFLUOROMETHYL)SULFANE; (4 METHYLBENZYL)(TRIFLUOROMETHYL)SULFANE; (4 NITROBENZYL)(TRIFLUOROMETHYL)SULFANE; (BIPHENYL 3 YLMETHYL)(TRIFLUOROMETHYL)SULFANE; (NAPHTHALEN 2 YLMETHYL)(TRIFLUOROMETHYL)SULFANE; 2 [(TRIFLUOROMETHYLTHIO)METHYL]BENZONITRILE; 4 [(TRIFLUOROMETHYLTHIO)METHYL]BENZONITRILE; 4 TRIFLUOROETHYLTHIO 7 METHOXYCOUMARIN; 5 CHLORO 3 [(TRIFLUOROMETHYLTHIO)METHYL]BENZO[B]THIOPHENE; BENZYL BROMIDE; BENZYL TRIFLUOROMETHYL SULFIDE; BENZYL(TRIFLUOROMETHYL)SULFANE; FUNCTIONAL GROUP; METHYL 4 [(TRIFLUOROMETHYLTHIO)METHYL]BENZOATE; ORGANOMETALLIC COMPOUND; SULFIDE; SULFUR DERIVATIVE; TRIFLUOROMETHYLTHIOCOPPER; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; NUCLEOPHILICITY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE; TEMPERATURE SENSITIVITY; TRIFLUOROMETHYLTHIOLATION;

EID: 84878928248     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.05.073     Document Type: Article

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