Cobalt-Catalyzed Enantioselective Alkynylation of Oxabicyclic Alkenes

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC
Lin-Wen Wei, Zhan-Cai Ma, Zhao Wang, Yu Zhao, Yuan Huang
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引用次数: 1

Abstract

An efficient access to enantioenriched cyclic homopropargylic alcohols through an unprecedented cobalt-catalyzed asymmetric alkynylation of oxabicyclic alkenes. By using inexpensive cobalt salt/chiral bisphosphine ligand as the catalyst and easy-to-handle potassium alkynyltrifluoroborates as the nucleophiles, synthetically valuable homopropargylic alcohols are obtained in moderate to good yields and high enantioselectivities.
钴催化氧三环烯烃的对映选择性炔基化
通过前所未有的钴催化的不对称氧杂环烯烃烷基化,有效地获得对映富集的环丙炔醇。以廉价的钴盐/手性双膦配体为催化剂,易处理的炔基三氟硼酸钾为亲核试剂,以中高收率和高对映选择性制备了具有合成价值的同丙醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Synthesis-Stuttgart
Synthesis-Stuttgart 化学-有机化学
CiteScore
4.50
自引率
7.70%
发文量
435
审稿时长
1 months
期刊介绍: SYNTHESIS is an international full-paper journal devoted to the advancement of the science of chemical synthesis. It covers all fields of organic chemistry involving synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines. SYNTHESIS provides dependable research results with detailed and reliable experimental procedures and full characterization of all important new products as well as scientific primary data.
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