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Ugi 反应和 Passerini 环封闭法合成人工大环

Artificial Macrocycles by Ugi Reaction and Passerini Ring Closure.

机构信息

Department of Drug Design, University of Groningen , A. Deusinglaan 1, 9713 AV Groningen, The Netherlands.

Chemistry Department, Faculty of Science, Sohag University , Sohag 82524, Egypt.

出版信息

J Org Chem. 2016 Oct 7;81(19):8789-8795. doi: 10.1021/acs.joc.6b01430. Epub 2016 Sep 15.

Abstract

Artificial macrocycles can be convergently synthesized by a sequence of an Ugi multicomponent reaction (MCR) followed by an intramolecular Passerini MCR used to close the macrocycle. Significantly, in this work, the first intramolecular macrocyclization through a Passerini reaction is described. We describe 21 macrocycles of a size of 15-20. The resulting macrocyclic depsipeptides are model compounds for natural products and could find applications in drug discovery.

摘要

人工大环可以通过一系列 Ugi 多组分反应 (MCR) 然后进行分子内 Passerini MCR 反应来进行收敛性合成,用于闭环大环。重要的是,在这项工作中,首次通过 Passerini 反应进行分子内大环化。我们描述了 21 个大小为 15-20 的大环。所得的大环环肽是天然产物的模型化合物,可在药物发现中找到应用。

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