过渡金属催化的缺电子π-不饱和体系的不对称不对称反应

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Xue Song , Shangde Liu , Wei Du , Ying-Chun Chen
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引用次数: 0

摘要

亲电性π-不饱和化合物的非极性反应是逆转固有极性,形成非常规键的有力策略。虽然有机的σ-路易斯碱催化剂是经典的使用,在这篇特约文章中,回顾了不同的电子贫不饱和体系,通常以二烯形式,通过氧化环金属化或π-路易斯碱活化机制进行的低价过渡金属介导的不对称不对称反应的最新进展。内容是根据过渡金属类别组织的,重点是催化机制,区域和立体选择性控制以及限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transition metal-catalysed asymmetric umpolung reactions of electron-deficient π-unsaturated systems

Transition metal-catalysed asymmetric umpolung reactions of electron-deficient π-unsaturated systems
The umpolung reaction of electrophilic π-unsaturated compounds represents a powerful strategy to reverse inherent polarity, enabling unconventional bond formations. While organic σ-Lewis base catalysts are classically utilised, in this feature article, recent advances in the low valent transition metal-mediated asymmetric umpolung reactions of diverse electron-poor unsaturated systems, usually in a diene form, are reviewed, proceeding through either an oxidative cyclometallation or a π-Lewis base activation mechanism. The contents are organised according to transition metal categories, with emphasis on catalytic mechanisms, regio- and stereoselectivity control, and limitations.
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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