期刊
SYNLETT
卷 32, 期 12, 页码 1151-1156出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0040-1705987
关键词
nickel catalysis; cross-coupling; cross-electrophile coupling; asymmetric synthesis; enantioselective synthesis
资金
- NIH NIGMS [R01GM100212]
- Allergan Graduate Fellowship
This article discusses the research conducted in the lab on the activation of alcohol derivatives in cross-coupling and cross-electrophile coupling reactions. The developed methods have enabled the use of secondary alcohols to produce tertiary stereogenic centers, which have been applied in the synthesis of pharmaceutically relevant compounds and substructures. The lab first focuses on the synthesis of bioactive compounds through stereospecific Kumada cross-coupling reactions and then discusses the development of a stereoselective cross-electrophile coupling reaction to synthesize cyclopropanes.
We discuss our laboratory's research in the activation of alcohol derivatives in cross-coupling and cross-electrophile coupling reactions. Our developed methods enable the use of secondary alcohols to afford tertiary stereogenic centers, which we applied to the synthesis of pharmaceutically relevant compounds and substructures. We first-discuss the synthesis of bioactive compounds through stereospecific Kumada cross-coupling reactions and follow this with a discussion on the development of our stereoselective cross-electrophile coupling-reaction to synthesize cyclopropanes.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据