Cu(OTf)2-catalyzed selective opening of aryl and vinyl epoxides with carbonyl compounds to give 1,3-dioxolanes

被引：13

作者：

Krasik, P ^{[1
]}

Bohemier-Bernard, M ^{[1
]}

Yu, Q ^{[1
]}

机构：

[1] Shire BioChem Inc, Laval, PQ H7V 4A7, Canada

来源：

SYNLETT | 2005年 / 05期

关键词：

epoxide-opening; dioxolanes; copper triflate; chemoselectivity;

D O I：

10.1055/s-2005-864795

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Copper(II) triflate catalyzes the ring-opening of aryl- and vinyl-substituted epoxides with various carbonyl compounds to furnish 1,3-dioxolanes under mild conditions. Alkyl- and alkoxy-carbonyl-substituted epoxides remain unchanged under reaction conditions. This allows selective opening of aryl-substituted epoxides in the presence of alkyl-substituted ones.

引用

收藏

页码：854 / 856

页数：3

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