| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5213930 | Tetrahedron | 2017 | 6 Pages |
Abstract
An efficient decarboxylative thioamidation of arylacetic and cinnamic acids has been developed employing formamides as amine surrogate and sulfur as promoter. Thioamides with variant structural features are obtained under mild reaction conditions without the use of transition metal catalysts and oxidants.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
