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Abstract：
The nudeophilic trifluoromethylthiolation of benzyl bromides using (bpy)Cu(SCF3) gave the desired products of benzyl trifluoromethyl sulfides in good to excellent yields. A diverse set of important functional groups including cyano, nitro, ester, alkoxy, halide, and heterocyclic groups can be well tolerated in the protocol. (C) 2013 Elsevier Ltd. All rights reserved.
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TETRAHEDRON
ISSN： 0040-4020
Year： 2013
Issue： 30
Volume： 69
Page： 6046-6050
2 . 8 1 7
JCR@2013
2 . 1 0 0
JCR@2023
ESI Discipline： CHEMISTRY;
JCR Journal Grade：2
CAS Journal Grade：3
Cited Count：
WoS CC Cited Count： 64
SCOPUS Cited Count： 67
ESI Highly Cited Papers on the List： 0 Unfold All
WanFang Cited Count：
Chinese Cited Count：
30 Days PV： 2
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