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氮杂环卡宾通过唑鎓二烯醇盐的催化:一种远程对映选择性功能化的有效策略。

N-Heterocyclic Carbene Catalysis via Azolium Dienolates: An Efficient Strategy for Remote Enantioselective Functionalizations.

机构信息

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

出版信息

Angew Chem Int Ed Engl. 2018 Apr 3;57(15):3862-3873. doi: 10.1002/anie.201709684. Epub 2018 Mar 9.

Abstract

N-heterocyclic carbene (NHC) catalysis has emerged as a powerful strategy in organic synthesis. In recent years a number of reviews have been published on NHC-catalyzed transformations involving Breslow intermediates, acyl azoliums, α,β-unsaturated acyl azoliums, homoenolate equivalents, and azolium enolates. However, the azolium dienolate intermediates generated by NHCs have been employed in asymmetric synthesis only very recently, especially in cycloadditions dealing with remote functionalization. This Minireview highlights all the developments and the new advances in NHC-catalyzed asymmetric cycloaddition reactions involving azolium dienolate intermediates.

摘要

氮杂环卡宾(NHC)催化已成为有机合成中的一种强大策略。近年来,已有多篇关于涉及 Breslow 中间体、酰基氮杂环丙烷、α,β-不饱和酰基氮杂环丙烷、偕烯醇化物等价物和氮杂环丙烷烯醇化物的 NHC 催化转化的综述发表。然而,氮杂环卡宾产生的氮杂环戊二烯醇盐中间体最近才被应用于不对称合成中,特别是在涉及远程官能化的环加成反应中。本综述重点介绍了涉及氮杂环戊二烯醇盐中间体的 NHC 催化不对称环加成反应的所有发展和新进展。

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