Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5268556 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
The reaction of α,β-unsaturated ketoximes with fluoroalkanosulfonyl fluorides in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) underwent the Beckmann rearrangement smoothly to afford the corresponding acid-sensitive enamides in moderate to excellent yields, which provides a new efficient method for the preparation of acid-sensitive enamides.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhaohua Yan, Yun Xu, Weisheng Tian,