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无配体微波辅助钯/铜催化的恶唑直接芳基化反应

Ligandless microwave-assisted Pd/Cu-catalyzed direct arylation of oxazoles.

作者信息

Besselièvre François, Mahuteau-Betzer Florence, Grierson David S, Piguel Sandrine

机构信息

Institut Curie/CNRS, UMR 176, Bât. 110-112, Centre Universitaire, Orsay F-91405, France.

出版信息

J Org Chem. 2008 Apr 18;73(8):3278-80. doi: 10.1021/jo7027135. Epub 2008 Mar 19.

Abstract

An efficient microwave-assisted palladium/copper co-mediated direct arylation of oxazoles with aryl bromides under ligandless conditions has been developed. The method is functional group tolerant and provides rapid access to medicinally relevant compounds in good yields. Coupled to the van Leusen oxazole ring synthesis, this methodology is illustrated by an expedient two-step synthesis of the four 2,5-diaryloxazole alkaloids texamine, texaline, balsoxin, and O-Me-halfordinol from commercially available starting materials.

摘要

已开发出一种高效的微波辅助钯/铜共介导的在无配体条件下恶唑与芳基溴的直接芳基化反应。该方法对官能团具有耐受性,能以良好的产率快速获得与药物相关的化合物。与范鲁森恶唑环合成法相结合,通过从市售起始原料简便地两步合成四种2,5 - 二芳基恶唑生物碱,即特沙明、特沙林、巴尔索辛和O - 甲基哈尔福迪诺,对该方法进行了说明。

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