Feng Minghao, Zhang Haoqi, Maulide Nuno
Faculty of Chemistry Institute of Organic Chemistry University of Vienna Währinger Straße 38 1090 Vienna Austria.
Christian-Doppler Laboratory for Entropy-Oriented Drug Design Josef-Holaubek-Platz 2 1090 Vienna Austria.
Angew Chem Weinheim Bergstr Ger. 2022 Dec 5;134(49):e202212213. doi: 10.1002/ange.202212213. Epub 2022 Nov 2.
In contrast to ketones and carboxylic esters, amides are classically seen as comparatively unreactive members of the carbonyl family, owing to their unique structural and electronic features. However, recent decades have seen the emergence of research programmes focused on the selective activation of amides under mild conditions. In the past four years, this area has continued to rapidly develop, with new advances coming in at a fast pace. Several novel activation strategies have been demonstrated as effective tools for selective amide activation, enabling transformations that are at once synthetically useful and mechanistically intriguing. This Minireview comprises recent advances in the field, highlighting new trends and breakthroughs in what could be called a new age of amide activation.
与酮类和羧酸酯不同,由于其独特的结构和电子特性,酰胺传统上被视为羰基家族中反应活性相对较低的成员。然而,近几十年来,出现了一些专注于在温和条件下选择性活化酰胺的研究项目。在过去四年中,这一领域持续快速发展,新进展层出不穷。几种新型活化策略已被证明是选择性酰胺活化的有效工具,能够实现既具有合成实用性又具有机理趣味性的转化。本综述涵盖了该领域的最新进展,突出了在可称为酰胺活化新时代的新趋势和突破。