Issue 45, 2016

Phosphine-free chiral iridium catalysts for asymmetric catalytic hydrogenation of simple ketones

Abstract

Novel pyridylalkylamine and aminopyridinato ligand stabilized iridium complexes with no P ligand are introduced. These complexes have been investigated as catalysts for asymmetric hydrogenation of simple ketones, resulting in an active catalyst for bulky alkyl aryl ketones that is α-methylpropiophenone. The ligands were synthesized from inexpensive starting materials and their modular design allows for the introduction of a broad variety of substitution patterns. Additionally, better activity and selectivity was observed at 20 °C and 20 bar H2 pressure with a catalyst loading as low as 0.05 mol% iridium. These phosphorus free catalysts have always been a central issue in both academic and industrial research.

Graphical abstract: Phosphine-free chiral iridium catalysts for asymmetric catalytic hydrogenation of simple ketones

Supplementary files

Article information

Article type
Paper
Submitted
19 Feb 2016
Accepted
04 Apr 2016
First published
05 Apr 2016
This article is Open Access
Creative Commons BY license

RSC Adv., 2016,6, 39335-39342

Author version available

Phosphine-free chiral iridium catalysts for asymmetric catalytic hydrogenation of simple ketones

P. Kumar, T. Irrgang, G. E. Kostakis and R. Kempe, RSC Adv., 2016, 6, 39335 DOI: 10.1039/C6RA04524C

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