| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5212142 | Tetrahedron | 2017 | 6 Pages |
Abstract
The reactivity of thiosulfonates with nucleophilic reagents was investigated. When reactions of thiosulfonates with thiols were performed, unsymmetrical disulfides were obtained in excellent yields. This procedure could employ numerous aryl or alkyl thiols. On the other hand, reactions of thiosulfonates with amines proceeded in the presence of a copper catalyst. The procedure was performed efficiently in air, and afforded the corresponding sulfenamides.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Nobukazu Taniguchi,