| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5226211 | Tetrahedron | 2009 | 7 Pages |
Abstract
A series of thiols have been examined as protic nucleophiles for Michael-type additions to α,β-unsaturated carbonyls as well as double nucleophilic condensations with aldehydes, ketones, and acetals catalyzed by amphoteric, water-tolerant vanadyl triflate under mild and neutral conditions. The newly developed C-S bond formation protocols were carried out smoothly in good to high yields in a highly chemoselective manner.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Chien-Tien Chen, Yow-Dzer Lin, Cheng-Yuan Liu,