金催化的后mcr转化为复杂(多)杂环

Q1 Pharmacology, Toxicology and Pharmaceutics
Upendra K. Sharma , Guilong Tian , Leonid G. Voskressensky , Erik V. Van der Eycken
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引用次数: 13

摘要

多组分后反应(Post - multicomponent reaction, MCR)转化是制备高结构多样性和分子复杂性的最成功方法之一。众所周知的MCR, Ugi反应通常提供线性肽骨架,使Ugi后转化成为一种优雅的解决方案,将Ugi加合物固化成更像药物的物种。毫不奇怪,在过去几年中,导致新结构框架的这种转变的发展迅速扩大。这些反应已经达到了令人印象深刻的性能和多功能性水平,特别是在与金的混合催化方面。这篇综述概述了过去十年中取得的发展,强调了以顺序或多米诺骨牌方式进行的修改,重点是主要概念,衍生产品的合成应用以及机械方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gold-catalyzed post-MCR transformations towards complex (poly)heterocycles

Gold-catalyzed post-MCR transformations towards complex (poly)heterocycles

Post multicomponent reaction (MCR) transformations are one of the most successful methods leading to high structural diversity and molecular complexity. A well-known MCR, the Ugi reaction typically affords a linear peptide backbone, enabling post-Ugi transformations as an elegant solution to rigidify the Ugi adduct into more drug-like species. Not surprisingly, the development of such transformations leading to new structural frameworks has expanded rapidly over the last few years. These reactions have reached an impressive level of performance and versatility, particularly in amalgamation with gold catalysis. This review outlines the developments achieved in the past decade, highlighting the modifications that are performed in a sequential or domino fashion with emphasis on major concepts, synthetic applications of the derived products as well as mechanistic aspects.

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来源期刊
Drug Discovery Today: Technologies
Drug Discovery Today: Technologies Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Discovery Today: Technologies compares different technological tools and techniques used from the discovery of new drug targets through to the launch of new medicines.
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