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通过钯催化烯丙基的氢炔基化反应制备 ()-1,3-烯炔衍生物。

Preparation of ()-1,3-Enyne Derivatives through Palladium Catalyzed Hydroalkynylation of Allenes.

机构信息

Department of Chemistry and Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian, PR China.

出版信息

J Org Chem. 2022 Jan 21;87(2):1589-1597. doi: 10.1021/acs.joc.1c02732. Epub 2021 Dec 30.

Abstract

A general and efficient palladium catalyzed hydroalkynylation of allenes was developed to produce synthetically versatile ()-1,3-enyne derivatives with high regio- and stereoselectivity. This catalytic system proceeded under mild conditions and was compatible with a broad range of substrates, especially for allenes without electron-bias groups. This work further broadens the synthetic potential of these scaffolds in organic synthesis and medicinal chemistry.

摘要

发展了一种通用且高效的钯催化丙炔基化反应,用于合成具有高区域和立体选择性的合成多功能()-1,3-烯炔衍生物。该催化体系在温和条件下进行,并且与广泛的底物兼容,特别是对于没有电子偏见基团的丙炔。这项工作进一步拓宽了这些支架在有机合成和药物化学中的合成潜力。

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