Issue 31, 2022

RuPHOX–Ru catalyzed asymmetric hydrogenation of α-substituted tetralones via a dynamic kinetic resolution

Abstract

The efficient RuPHOX–Ru catalyzed asymmetric hydrogenation of α-substituted tetralones via a dynamic kinetic resolution has been achieved for the synthesis of chiral tetrahydronaphthols. The mechanism study indicated that hydrogenation with H2 gas, rather than transfer hydrogenation with EtOH solvent as the hydrogen source, predominates in the reaction pathway.

Graphical abstract: RuPHOX–Ru catalyzed asymmetric hydrogenation of α-substituted tetralones via a dynamic kinetic resolution

Supplementary files

Article information

Article type
Communication
Submitted
27 Feb 2022
Accepted
23 Mar 2022
First published
23 Mar 2022

Chem. Commun., 2022,58, 4905-4908

RuPHOX–Ru catalyzed asymmetric hydrogenation of α-substituted tetralones via a dynamic kinetic resolution

J. Li, J. Ye, J. Zhou, J. Li, D. Liu and W. Zhang, Chem. Commun., 2022, 58, 4905 DOI: 10.1039/D2CC01193J

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