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螺哌啶类化合物的合成策略——近 10 年的研究进展综述。

Strategies for the synthesis of spiropiperidines - a review of the last 10 years.

机构信息

Department of Chemistry, University of York, Heslington, York, YO10 5DD, UK.

出版信息

Org Biomol Chem. 2018 Sep 19;16(36):6620-6633. doi: 10.1039/c8ob01271g.

Abstract

Spiropiperidines have gained in popularity in drug discovery programmes as medicinal chemists explore new areas of three-dimensional chemical space. This review focuses on the methodology used for the construction of 2-, 3- and 4-spiropiperidines, covering the literature from the last 10 years. It classifies the synthesis of each of the types of spiropiperidine by synthetic strategy: the formation of the spiro-ring on a preformed piperidine ring, and the formation of the piperidine ring on a preformed carbo- or heterocyclic ring. While 3- and 4-spiropiperidines are predominantly synthesised for drug discovery projects, 2-spiropiperidines are synthesised en route to natural products. The lack of 2-spiropiperidines in drug discovery is presumably due to limited general procedures for their synthesis.

摘要

螺环哌啶类化合物在药物研发项目中越来越受欢迎,因为药物化学家正在探索三维化学空间的新领域。本综述重点介绍了过去 10 年用于构建 2-、3-和 4-螺环哌啶的方法学。它根据合成策略对每种螺环哌啶的合成进行了分类:在预先形成的哌啶环上形成螺环,以及在预先形成的碳环或杂环上形成哌啶环。虽然 3-和 4-螺环哌啶主要用于药物发现项目的合成,但 2-螺环哌啶则用于天然产物的合成。在药物发现中缺乏 2-螺环哌啶可能是由于其合成的一般程序有限。

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