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通过不对称联芳偶联反应的全合成手性联芳天然产物。

Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling.

机构信息

Department of Chemistry, Roy and Diana Vagelos Laboratoies, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, USA.

出版信息

Chem Soc Rev. 2009 Nov;38(11):3193-207. doi: 10.1039/b821092f. Epub 2009 Sep 23.

Abstract

This tutorial review highlights the use of catalytic asymmetric 2-naphthol couplings in total synthesis. The types of chirality, chiral biaryl natural products, prior approaches to chiral biaryl natural products, and other catalytic asymmetric biaryl couplings are outlined. The three main categories of chiral catalysts for 2-naphthol coupling (Cu, V, Fe) are described with discussion of their limitations and advantages. Applications of the copper catalyzed couplings in biomimetic syntheses are discussed including nigerone, hypocrellin, calphostin D, phleichrome, and cercosporin.

摘要

本教程综述强调了催化不对称 2-萘酚偶联在全合成中的应用。概述了手性类型、手性联芳基天然产物、手性联芳基天然产物的先前方法以及其他催化不对称联芳基偶联。描述了用于 2-萘酚偶联的三种主要手性催化剂(铜、钒、铁)类别,并讨论了它们的局限性和优点。讨论了铜催化偶联在生物模拟合成中的应用,包括尼日酮、血根碱、calphostin D、phleichrome 和 cercosporin。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2423/2904069/cee408edd4e9/nihms-215475-f0001.jpg

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