Schramm, York and Barrios-Landeros, Fabiola and Pfaltz, Andreas. (2013) Discovery of an Iridacycle Catalyst with Improved Reactivity and Enantioselectivity in the Hydrogenation of Dialkyl Ketimines. Chemical Science, 4. pp. 2760-2766.
|
PDF
- Published Version
Available under License CC BY (Attribution). 602Kb |
Official URL: http://edoc.unibas.ch/dok/A6212007
Downloads: Statistics Overview
Abstract
Catalytically active iridacycles are formed by cyclometalation of acetophenone imines with Ir-PHOX complexes under hydrogen atmosphere. These complexes show unusually high reactivity and enantioselectivity in the hydrogenation of alkyl methyl ketimines. The structure of the cyclometalated imine has a strong effect on the conversion and enantiomeric excess.
Faculties and Departments: | 05 Faculty of Science 05 Faculty of Science > Departement Chemie > Former Organization Units Chemistry > Synthetische organische Chemie (Pfaltz) |
---|---|
UniBasel Contributors: | Pfaltz, Andreas |
Item Type: | Article, refereed |
Article Subtype: | Research Article |
Publisher: | Royal Society of Chemistry |
ISSN: | 2041-6520 |
e-ISSN: | 2041-6539 |
Note: | Publication type according to Uni Basel Research Database: Journal article |
Language: | English |
Identification Number: |
|
edoc DOI: | |
Last Modified: | 10 Apr 2017 08:57 |
Deposited On: | 31 Jan 2014 09:51 |
Repository Staff Only: item control page