Literature DB >> 18563909

An efficient copper-aluminum hydrotalcite catalyst for asymmetric hydrosilylation of ketones at room temperature.

M Lakshmi Kantam1, Soumi Laha, Jagjit Yadav, Pravin R Likhar, Bojja Sreedhar, Shailendra Jha, Suresh Bhargava, M Udayakiran, B Jagadeesh.   

Abstract

A catalyst system consisting of a copper-aluminum hydrotalcite-chiral diphosphine ligand effects asymmetric hydrosilylation of several ketones, using polymethylhydrosiloxane (PMHS) as the stoichiometric reducing agent at room temperature, with moderate-to-excellent enantioselectivities. The catalyst is recovered by simple centrifugation, and the efficiency of the catalyst remains almost unaltered even after several cycles.

Entities:  

Year:  2008        PMID: 18563909     DOI: 10.1021/ol800616p

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  A Comparative Study on Asymmetric Reduction of Ketones Using the Growing and Resting Cells of Marine-Derived Fungi.

Authors:  Hui Liu; Bi-Shuang Chen; Fayene Zeferino Ribeiro de Souza; Lan Liu
Journal:  Mar Drugs       Date:  2018-02-14       Impact factor: 5.118

2.  Immobilized and Free Cells of Geotrichum candidum for Asymmetric Reduction of Ketones: Stability and Recyclability.

Authors:  Hui Liu; Fayene Zeferino Ribeiro de Souza; Lan Liu; Bi-Shuang Chen
Journal:  Molecules       Date:  2018-08-27       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.