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首页> 外文期刊>Angewandte Chemie >Highly Enantioselective Organocatalytic Carbonyl-Ene Reaction with Strongly Acidic,Chiral Bronsted Acids as Efficient Catalysts
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Highly Enantioselective Organocatalytic Carbonyl-Ene Reaction with Strongly Acidic,Chiral Bronsted Acids as Efficient Catalysts

机译:与强酸性手性布朗斯台德酸的高对映选择性有机催化羰基-烯反应作为高效催化剂

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摘要

Asymmetric Bronsted acid catalysis has emerged as a powerful tool in organic synthesis.In particular,chiral phosphoric acids have become established as useful organocatalysts for highly enantioselective transformations.The central role performed by the phosphoric acids in such reactions is the activation of the electrophile by catalytic protonation to form an intermediary ion pair composed of the activated(proton-ated)electrophile and a chiral phosphate counterion.This counterion induces the high enantioselectivities observed.Various enantioselective transformations of aldimines and ketimines have been carried out by applying this strategy.
机译:不对称布朗斯台德酸催化已成为有机合成中的有力工具,特别是手性磷酸已被确立为用于高对映选择性转化的有用有机催化剂。磷酸在此类反应中的主要作用是通过催化活化亲电子质子化形成由活化的(质子化的)亲电子体和手性磷酸抗衡离子组成的中间离子对,该抗衡离子诱导观察到的高对映选择性。通过应用该策略进行了各种对映体的醛亚胺和酮亚胺转化。

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