金属烯醇酯不对称合成四元立体中心

Katerina M. Korch, Steven A. Loskot, B. Stoltz
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引用次数: 2

摘要

在各种不对称转化中使用手性金属烯醇酯中间体的策略已经允许产生四元立体中心产品,否则难以获得。许多经典的转化,包括醛醇、曼尼希、共轭加成、烷基化和环型反应,以及烯丙基烷基化和α-芳基化/烯基化,已经适应于通过手性金属烯醇酯中间体进行,允许在分子间和分子内不对称合成许多复杂产物。这些转化已被证明在天然产物的合成中是有用的,并且将来也可能应用于合成新药和其他感兴趣的化合物。该审查包括截至2014年并包括2014年的工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Asymmetric Synthesis of Quaternary Stereocenters via Metal Enolates
The strategy of using chiral metal enolate intermediates in a diverse variety of asymmetric transformations has allowed the generation of quaternary stereocenter-bearing products that are otherwise difficult to access. Many classic transformations including aldol, Mannich, conjugate addition, alkylation, and pericyclic-type reactions, as well as allylic alkylation and α-arylation/alkenylation, have been adapted to proceed through chiral metal enolate intermediates, allowing the asymmetric synthesis of many complex products in both an intermolecular and intramolecular manner. These transformations have proven useful in the synthesis of natural products and may also be applied to the synthesis of novel pharmaceuticals and other compounds of interest in the future. This review includes work done up to and including the year 2014.
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