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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Lewis base catalysis of three n-π* mediated reactions with N-heterocyclic carbenes (NHCs), isothioureas, bicyclic tertiary amines, and electron-rich pyridyls
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Lewis base catalysis of three n-π* mediated reactions with N-heterocyclic carbenes (NHCs), isothioureas, bicyclic tertiary amines, and electron-rich pyridyls

机译:Lewis碱催化与N-杂环卡宾(NHC),异硫脲,双环叔胺和富电子吡啶基的三个n-π*介导的反应

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摘要

Lewis base catalysis by lone pair donation into anti-bonding π orbitals (n-π*) is a growing field with a range of Lewis bases capable of this type of catalysis. In this review, catalysis of the Morita-Baylis-Hillman reaction, the Steglich rearrangement, and the annulation of α,β- unsaturated acyl Lewis adducts are discussed, using N-heterocyclic carbene (NHC), isothiourea, bicyclic tertiary amine and electron-rich pyridyl catalysts. In many cases, each of these popular Lewis base catalysts is viable for the given reaction, with the degree of utility defined by the catalyst's nucleophilicity and Lewis basicity. 1 Introduction to Lewis Base Catalysis 2 Enolates from 1,4-Addition: Morita-Baylis-Hillman Reaction 3 O→C Carboxyl Transfer: Steglich Rearrangement 4 Annulations of α,β-Unsaturated Acyl Lewis Base Adducts 5 Summary and Outlook
机译:通过孤对捐赠进入反键π轨道(n-π*)的路易斯碱催化是一个不断发展的领域,具有一系列能够进行这种催化作用的路易斯碱。在这篇综述中,我们讨论了使用N-杂环卡宾(NHC),异硫脲,双环叔胺和电子-对Morita-Baylis-Hillman反应的催化,Steglig重排以及α,β-不饱和酰基路易斯Lewis加合物的环化反应。丰富的吡啶基催化剂。在许多情况下,这些流行的路易斯碱催化剂中的每一种对于给定的反应都是可行的,其实用程度由催化剂的亲核性和路易斯碱性确定。 1 Lewis碱催化入门2从1,4-加成中得到的烯醇化:Morita-Baylis-Hillman反应3 O→C羧基转移:Steglich重排4α,β-不饱和酰基Lewis碱加合物的环状结构5概述和展望

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