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[2.2]基于对环芳烷的异硫脲催化的羧酸高度对映选择性α-氟化反应

[2.2]Paracyclophane-Based Isothiourea-Catalyzed Highly Enantioselective α-Fluorination of Carboxylic Acids.

作者信息

Yuan Shiru, Liao Chen, Zheng Wen-Hua

机构信息

State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, 163 Xianlin Avenue, Nanjing 210023, Jiangsu, China.

出版信息

Org Lett. 2021 Jun 4;23(11):4142-4146. doi: 10.1021/acs.orglett.1c01046. Epub 2021 May 14.

Abstract

Planar chiral [2.2]paracyclophane-based isothiourea catalysts have been prepared over a few simple steps in high yields. In the presence of these catalysts, highly efficient catalytic enantioselective fluorination of carboxylic acids has been accomplished, providing a broad range of optically active α-fluoroesters in high yield and excellent enantioselectivity.

摘要

基于平面手性[2.2]对环芳烷的异硫脲催化剂可通过几个简单步骤高收率制备。在这些催化剂存在下,已实现了羧酸的高效催化对映选择性氟化反应,以高收率和优异的对映选择性提供了多种光学活性α-氟代酯。

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