Suppr超能文献

手性黄烷-3-醇的不对称合成。

Asymmetric Synthesis of Chiral Flavan-3-Ols.

机构信息

a Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China , Hengyang , Hunan , PR China.

b Institute of Pharmacy & Pharmacology, University of South China , Hengyang , Hunan , PR China.

出版信息

Nat Prod Res. 2019 Oct;33(20):2995-3010. doi: 10.1080/14786419.2018.1509337. Epub 2018 Dec 6.

Abstract

Flavan-3-ols are a series of natural products widely present in plants and show versatile biological activities. The structures of such compounds are characterized by owing two adjacent chiral centers and three rings. Their interesting structures and promising biological activities have driven increasing research developments toward the preparation of enantioenriched flavan-3-ols. This review summarizes the recent approaches for the asymmetric synthesis of chiral flavan-3-ols from two strategies in the construction of chiral centers. The key steps in the synthetic protocol involve Sharpless asymmetric dihydroxylation, Shi asymmetric epoxidation and Sharpless asymmetric epoxidation.

摘要

黄烷-3-醇是广泛存在于植物中的一系列天然产物,具有多种生物活性。这些化合物的结构特点是含有两个相邻的手性中心和三个环。它们有趣的结构和有前途的生物活性促使人们越来越多地研究手性黄烷-3-醇的制备方法。本文综述了近年来从构建手性中心的两个策略出发,不对称合成手性黄烷-3-醇的最新方法。合成方案中的关键步骤包括 Sharpless 不对称双羟化、Shi 不对称环氧化和 Sharpless 不对称环氧化。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验