Issue 28, 2011

Asymmetric hydrogenation of alkenes lacking coordinating groups

Abstract

Asymmetric hydrogenation of olefins is one of the most important reactions for the synthesis of optically active compounds, especially in industry. Chiral iridium catalysts based on P,N ligands have strongly expanded their application range. In contrast to rhodium and ruthenium diphosphine complexes they do not require the presence of a coordinating group near the C[double bond, length as m-dash]C bond and, therefore, allow highly enantioselective hydrogenations of largely unfunctionalized alkenes.

Graphical abstract: Asymmetric hydrogenation of alkenes lacking coordinating groups

Article information

Article type
Highlight
Submitted
11 Mas 2011
Accepted
12 Eph 2011
First published
10 Mey 2011

Chem. Commun., 2011,47, 7912-7916

Asymmetric hydrogenation of alkenes lacking coordinating groups

D. H. Woodmansee and A. Pfaltz, Chem. Commun., 2011, 47, 7912 DOI: 10.1039/C1CC11430A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements