| Literature DB >> 24712689 |
Santosh Agrawal1, Elisa Martínez-Castro, Rocío Marcos, Belén Martín-Matute.
Abstract
A ruthenium complex formed from commercially available [Ru(p-cymene)Cl2]2 and 1,4-bis(diphenylphosphino)butane catalyzes the racemization of aromatic α-hydroxy ketones very efficiently at room temperature. The racemization is fully compatible with a kinetic resolution catalyzed by a lipase from Pseudomonas stutzeri. This is the first example of dynamic kinetic resolution of α-hydroxy ketones at ambient temperature in which the metal and enzyme catalysts work in concert in one pot at room temperature to give quantitative yields of esters of α-hydroxy ketones with very high enantioselectivity.Entities:
Year: 2014 PMID: 24712689 DOI: 10.1021/ol500764q
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005