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Iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones to chiral diols†
Xiao-Hui Yang,Hai-Tao Yue,Na Yu,Yi-Pan Li,Jian-Hua Xie
Chemical Science Pub Date : 11/15/2016 00:00:00 , DOI:10.1039/C6SC04609F
Abstract

We report a protocol for the highly efficient iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones via dynamic kinetic resolution. Using Ir-SpiroPAP (R)-1d as a catalyst, a wide range of chiral diols were prepared in a high yield (80–95%) with a high enantioselectivity (up to 95% ee) under mild reaction conditions. This protocol was used for enantioselective syntheses of (−)-preclamol and a chiral 2,5-disubstituted tetrahydropyran.

Graphical abstract: Iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones to chiral diols
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