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α-酮酸:有机合成中的酰化试剂。

α-Keto Acids: Acylating Agents in Organic Synthesis.

机构信息

Laboratório de Síntese Orgânica Limpa - LASOL - CCQFA - Universidade Federal de Pelotas - UFPel, P.O. Box 354, 96010-900 Pelotas, RS, Brazil.

出版信息

Chem Rev. 2019 Jun 26;119(12):7113-7278. doi: 10.1021/acs.chemrev.8b00782. Epub 2019 Apr 16.

Abstract

A significant number of important acyl-transfer reactions, such as direct acylation, acylation, heteroatom acylation, and a diversity of cyclization reactions using the title compound as a key starting material, have been described in recent years. Just like a sleeping beauty, α-oxocarboxylic acids were awakened from a 17-year sleep to become important reagents in classical and new acylation reactions. The greener characteristic of the coproduct formed in reactions using α-keto acid (only CO), together with its versatility as a building block in catalytic organic synthesis, accredit it as a candidate to green acylating agent, an alternative to acyl chloride, and other acyl-transfer reagents. This review presents the impressive breakthroughs achieved mainly in the past decade in the development of new catalytic reactions for the formation of C-C, C-N, and C-S bonds using α-keto acids.

摘要

近年来,已经有大量的重要酰基转移反应被描述,如直接酰化、酰化、杂原子酰化,以及使用标题化合物作为关键起始原料的多种环化反应。就像睡美人一样,α-氧代羧酸从沉睡了 17 年中苏醒过来,成为经典和新型酰化反应中的重要试剂。在使用α-酮酸(仅 CO)的反应中形成的副产物的绿色特性,以及其作为催化有机合成中构建块的多功能性,使它成为绿色酰化剂、酰氯和其他酰基转移试剂的替代品的候选物。这篇综述主要介绍了过去十年中在使用α-酮酸形成 C-C、C-N 和 C-S 键的新催化反应方面取得的令人瞩目的突破。

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