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钌(II)卟啉和简单的铜盐催化的 2,5-取代恶唑和恶唑啉的合成。

Synthesis of 2,5-disubstituted oxazoles and oxazolines catalyzed by ruthenium(II) porphyrin and simple copper salts.

机构信息

Key Laboratory of Drug-Targeting and Drug-Delivery Systems of the Ministry of Education, Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, Chengdu, Sichuan, 610041, P. R. China.

出版信息

J Org Chem. 2012 May 4;77(9):4271-7. doi: 10.1021/jo202663n. Epub 2012 Apr 17.

Abstract

A novel and moderate synthesis of 2,5-disubstituted oxazoles and oxazolines involving ruthenium(II) porphyrin-copper chloride catalyzed cyclization was developed. These reactions using readily available benzene carboxylic acids and phenylethenes or phenylacetylenes are performed under mild conditions. The reactions proceed in series, giving rise to the formation of an intermolecular C-N bond and an intramolecular C-O bond, which yield oxazole or oxazoline derivatives simultaneously.

摘要

发展了一种新型温和的 2,5-取代恶唑和恶唑啉的合成方法,涉及钌(II)卟啉-氯化铜催化的环化反应。这些反应使用易得的苯羧酸和苯乙烯或苯乙炔在温和条件下进行。反应依次进行,形成分子间 C-N 键和分子内 C-O 键,同时生成恶唑或恶唑啉衍生物。

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