Issue 60, 2022

Highly efficient and enantioselective synthesis of chiral lactones via Ir-catalysed asymmetric hydrogenation of ketoesters

Abstract

Owing to the biological significance and great synthetic value of chiral lactones and their derivatives, increasing attention has been paid to developing effective synthetic methods for chiral lactones. We herein report an efficient asymmetric hydrogenation of benzo-fused ketoesters, γ-ketoesters and biaryl-bridged ketoesters catalyzed by chiral iridium complexes bearing ferrocene-based chiral ligands, furnishing a series of chiral lactones in superb yields and excellent enantioselectivities (up to 99% yields and up to 99% ee).

Graphical abstract: Highly efficient and enantioselective synthesis of chiral lactones via Ir-catalysed asymmetric hydrogenation of ketoesters

Supplementary files

Article information

Article type
Communication
Submitted
11 Apr 2022
Accepted
07 Jun 2022
First published
09 Jun 2022

Chem. Commun., 2022,58, 8408-8411

Highly efficient and enantioselective synthesis of chiral lactones via Ir-catalysed asymmetric hydrogenation of ketoesters

J. Song, C. Yin, Y. Zhang, Y. Shi, Y. Li, G. Chen and X. Zhang, Chem. Commun., 2022, 58, 8408 DOI: 10.1039/D2CC02069F

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