Issue 10, 2022

Chiral FLP-catalyzed asymmetric hydrogenation of 3-fluorinated chromones

Abstract

The asymmetric hydrogenation of fluorinated olefins is an efficient pathway towards the synthesis of chiral fluorine-containing compounds. This paper described metal-free asymmetric hydrogenation of 3-fluorinated chromones with the use of readily available achiral borane and chiral oxazoline as an FLP catalyst for the first time. A variety of optically active 3-fluorochroman-4-ones were obtained in high yields with up to 88% ee.

Graphical abstract: Chiral FLP-catalyzed asymmetric hydrogenation of 3-fluorinated chromones

Supplementary files

Article information

Article type
Communication
Submitted
10 Dec 2021
Accepted
23 Dec 2021
First published
24 Dec 2021

Chem. Commun., 2022,58, 1558-1560

Chiral FLP-catalyzed asymmetric hydrogenation of 3-fluorinated chromones

Y. Dai, W. Meng, X. Feng and H. Du, Chem. Commun., 2022, 58, 1558 DOI: 10.1039/D1CC06964K

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