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布朗斯特酸催化的炔丙基化/环异构化串联反应:由炔丙醇和酰胺一锅法合成取代恶唑

Brønsted acid-catalyzed propargylation/cycloisomerization tandem reaction: one-pot synthesis of substituted oxazoles from propargylic alcohols and amides.

作者信息

Pan Ying-ming, Zheng Fei-jian, Lin Hai-xin, Zhan Zhuang-ping

机构信息

Department of Chemistry, College of Chemistry and Chemical Engineering, and State Key Laboratory for Physical Chemistry of Solid Surfaces, Xiamen University, Xiamen 361005, People's Republic of China.

出版信息

J Org Chem. 2009 Apr 17;74(8):3148-51. doi: 10.1021/jo8027533.

Abstract

An efficient one-pot propargylation/cycloisomerization tandem process has been developed for the synthesis of substituted oxazole derivatives from propargylic alcohols and amides with use of p-toluenesulfonic acid monohydrate (PTSA) as a bifunctional catalyst. This method provides a rapid and efficient access to substituted oxazoles.

摘要

已开发出一种高效的一锅法炔丙基化/环异构化串联过程,以对甲苯磺酸一水合物(PTSA)作为双功能催化剂,从炔丙醇和酰胺合成取代恶唑衍生物。该方法为合成取代恶唑提供了一种快速有效的途径。

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