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铜(II)六氟硫酸盐催化末端烯烃和炔丙醇的原子经济性化学选择性合成 1,4-烯炔。

Atom-economical chemoselective synthesis of 1,4-enynes from terminal alkenes and propargylic alcohols catalyzed by Cu(OTf)2.

机构信息

Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), School of Chemistry & Chemical Engineering of Guangxi Normal University, Guilin 541004, People's Republic of China.

出版信息

J Org Chem. 2013 Mar 15;78(6):2742-5. doi: 10.1021/jo3026803. Epub 2013 Feb 13.

DOI:10.1021/jo3026803
PMID:23379769
Abstract

A novel and efficient Cu(OTf)2-catalyzed sp(3)-sp(2) C-C bond formation reaction through the direct coupling of propargylic alcohols with terminal alkenes has been realized under mild conditions. The reaction is tolerant to air and is atom-economical, in accordance with the concept of modern green chemistry. The present protocol provides an attractive approach to a diverse range of 1,4-enynes in high to excellent yields.

摘要

一种新型、高效的铜(OTf)2 催化的 sp(3)-sp(2) C-C 键形成反应,通过炔丙醇与末端烯烃的直接偶联,在温和条件下实现。该反应对空气具有耐受性,且原子经济性高,符合现代绿色化学的理念。本方案为各种 1,4-烯炔提供了一种有吸引力的合成途径,产率高至优秀。

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