Asymmetric Autocatalysis as an Efficient Link Between the Origin of Homochirality and Highly Enantioenriched Compounds.

IF 1.2
Kenso Soai, Tsuneomi Kawasaki, Arimasa Matsumoto
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Abstract

Biological homochirality of essential components such as L-amino acids and D-sugars is prerequisite for the emergence, evolution and the maintenance of life. Implication of biological homochirality is described. Considerable interest has been focused on the origin and the process leading to the homochirality. Asymmetric autocatalysis with amplification of enantiomeric excess (ee), i.e., the Soai reaction, is capable to link the low ee induced by the proposed origins of chirality such as circularly polarized light and high ee of the organic compound. Absolute asymmetric synthesis without the intervention of any chiral factor was achieved in the Soai reaction.

Abstract Image

不对称自催化是同手性和高对映体富集化合物的有效联系。
l -氨基酸和d -糖等基本成分的生物同手性是生命出现、进化和维持的先决条件。描述了生物同手性的含义。人们对同手性的起源和形成过程一直很感兴趣。对映体过量(ee)扩增的不对称自催化,即Soai反应,能够将手性来源(如圆偏振光)和有机化合物的高ee诱导的低ee联系起来。在Soai反应中实现了无手性因子干预的绝对不对称合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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