| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268240 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Various α-keto-1,3,4-oxadiazole derivatives were synthesized through a sequential intermolecular dehydrochlorination/intramolecular aza-Wittig reaction of carboxylic acids and imidoyl chloride intermediates, which were generated by isocyanide-Nef reaction of acyl chlorides and (N-isocyanimine) triphenylphosphorane (1) in CH2Cl2 at room temperature.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Liren Cui, Qiong Liu, Jingxun Yu, Chongzhi Ni, Hui Yu,