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对映体纯锂酰胺作为手性氨等价物的共轭加成，第3部分:2012-2017

Q2 Chemistry
Tetrahedron, asymmetry Pub Date : 2017-12-15 DOI:10.1016/j.tetasy.2017.10.031
Stephen G. Davies, Ai M. Fletcher, Paul M. Roberts, James E. Thomson
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引用次数: 0

摘要

本文综述了对映体纯锂酰胺作为手性氨当量的共轭加成在不对称合成中的进一步应用，并提供了自2012年发表的上一篇综述以来的最新进展。
本文章由计算机程序翻译，如有差异，请以英文原文为准。

The conjugate addition of enantiomerically pure lithium amides as chiral ammonia equivalents part III: 2012–2017

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The conjugate addition of enantiomerically pure lithium amides as chiral ammonia equivalents part III: 2012–2017

This review covers further applications of the conjugate addition of enantiomerically pure lithium amides as chiral ammonia equivalents in asymmetric synthesis and provides an update since our last review of this area, which was published in 2012.

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来源期刊
Tetrahedron, asymmetry
Tetrahedron, asymmetry 化学-无机化学与核化学
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
1 months
期刊介绍： Cessation. Tetrahedron: Asymmetry presents experimental or theoretical research results of outstanding significance and timeliness on asymmetry in organic, inorganic, organometallic and physical chemistry, as well as its application to related disciplines, especially bio-organic chemistry. The journal publishes critical reviews, original research articles and preliminary communications dealing with all aspects of the chemical, physical and theoretical properties of non-racemic organic and inorganic materials and processes. Topics relevant to the journal include: the physico-chemical and biological properties of enantiomers; strategies and methodologies of asymmetric synthesis; resolution; chirality recognition and enhancement; analytical techniques for assessing enantiomeric purity and the unambiguous determination of absolute configuration; and molecular graphics and modelling methods for interpreting and predicting asymmetric phenomena. Papers describing the synthesis or properties of non-racemic molecules will be required to include a separate statement in the form of a Stereochemistry Abstract, for publication in the same issue, of the criteria used for the assignment of configuration and enantiomeric purity.
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