| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218023 | Tetrahedron | 2013 | 5 Pages |
Abstract
The nucleophilic 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.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Dedao Kong, Zhou Jiang, Shaogang Xin, Zhengshuai Bai, Yaofeng Yuan, Zhiqiang Weng,