1993
DOI: 10.1016/s0022-1139(00)80569-2
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Novel reactions of perfluoro-2-(trifluoromethyl)-propene

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Cited by 11 publications
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“…Vinyl trifluoromethyl sulfide can be prepared by the trifluoromethanesulfenylation of different substrates. The reaction of vinyl bromide with CuSCF 3 gave the corresponding trifluoromethyl sulfides (eqs a and b, Scheme ). , For the gem -dibromovinyl substrate, both monosubstituted and bisubstituted products were obtained (eq b, Scheme ) . Copper-catalyzed trifluoromethanesulfenylation of vinyl boronic acids with nucleophilic or electrophilic trifluoromethanesulfenylating reagents was reported by Vicic (eq c, Scheme ) and Shen (eq d, Scheme ), respectively.…”
Section: Synthesis Of C-scf3 Compoundsmentioning
confidence: 97%
“…Vinyl trifluoromethyl sulfide can be prepared by the trifluoromethanesulfenylation of different substrates. The reaction of vinyl bromide with CuSCF 3 gave the corresponding trifluoromethyl sulfides (eqs a and b, Scheme ). , For the gem -dibromovinyl substrate, both monosubstituted and bisubstituted products were obtained (eq b, Scheme ) . Copper-catalyzed trifluoromethanesulfenylation of vinyl boronic acids with nucleophilic or electrophilic trifluoromethanesulfenylating reagents was reported by Vicic (eq c, Scheme ) and Shen (eq d, Scheme ), respectively.…”
Section: Synthesis Of C-scf3 Compoundsmentioning
confidence: 97%