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

Shiru Yuan, Chen Liao, Wen‐Hua Zheng

2021Organic Letters32 citationsDOI

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.

Topics & Concepts

Enantioselective synthesisChemistryCatalysisYield (engineering)Optically activeCombinatorial chemistryOrganic chemistryMaterials scienceMetallurgyFluorine in Organic ChemistryInorganic Fluorides and Related CompoundsPorphyrin and Phthalocyanine Chemistry
[2.2]Paracyclophane-Based Isothiourea-Catalyzed Highly Enantioselective α-Fluorination of Carboxylic Acids | Litcius