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手性有机催化对映选择性合成芳基对醌:多样性导向合成联芳二醇的平台分子。

Organocatalytic Enantioselective Synthesis of Atropisomeric Aryl-p-Quinones: Platform Molecules for Diversity-Oriented Synthesis of Biaryldiols.

机构信息

Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen, 518055, China.

Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Shenzhen, 518055, China.

出版信息

Angew Chem Int Ed Engl. 2020 Jul 6;59(28):11374-11378. doi: 10.1002/anie.202004671. Epub 2020 May 7.

Abstract

Presented here is a class of novel axially chiral aryl-p-quinones as platform molecules for the preparation of non-C symmetric biaryldiols. Two sets of aryl-p-quinone frameworks were synthesized with remarkable enantiocontrol by means of chiral phosphoric acid catalyzed enantioselective arylation of p-quinones by central-to-axial chirality conversion. These aryl-p-quinones were then used to access a wide spectrum of highly functionalized non-C symmetric biaryldiols with excellent retention of the enantiopurity.

摘要

这里呈现了一类新型的轴向手性芳基-对醌作为平台分子,用于制备非中心对称联苯二醇。通过手性磷酸催化的对醌的中心到轴向手性转换的对映选择性芳基化反应,合成了两组具有显著对映控制的芳基-对醌框架。然后,这些芳基-对醌被用于获得广泛的高度官能化的非中心对称联苯二醇,对映纯度保持优异。

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