Organocatalytic Atroposelective Reactions of Alkynes

Synthesis Pub Date : 2024-01-09 DOI:10.1055/a-2241-3571
Zhi-Xin Zhang, Tian-Qi Hu, Long-Wu Ye, Bo Zhou
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Abstract

The atroposelective transformation of alkynes is an efficient protocol for the assembly of axially chiral compounds. Benefit from the rapid development of chiral organocatalysts, the organocatalytic atroposelective reactions of alkynes have been extensively studied during the past decades. An array of chiral catalysts, including chiral Brønsted acid catalysts, secondary amine catalysts, N-heterocyclic carbene (NHC) catalysts, thiourea catalysts and N-squaramide catalysts, were employed into the enantioselective reactions of different alkynes. This review summarizes the recent advances in organocatalytic atroposelective reactions of alkynes according to the types of alkyne substrates. The reaction mechanisms, mode of enantiocontrol, product diversity and applications are highlighted in this review.
炔烃的有机催化逆选择反应
炔烃的反向选择性转化是组装轴向手性化合物的有效方法。得益于手性有机催化剂的快速发展,在过去的几十年中,人们对炔烃的有机催化反选择反应进行了广泛的研究。一系列手性催化剂,包括手性布氏酸催化剂、仲胺催化剂、N-杂环碳烯(NHC)催化剂、硫脲催化剂和 N-夸父酰胺催化剂,被用于不同炔烃的对映选择性反应。本综述根据炔基质的类型总结了炔烃有机催化对映体选择性反应的最新进展。本综述重点介绍了反应机理、对映控制模式、产物多样性和应用。
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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