Issue 2, 2007

Enantioselective synthesis of β2-amino acids using rhodium-catalyzed hydrogenation

Abstract

A series of protected β2-dehydroamino acids has been prepared in three steps from commercially available starting materials in good yields. These were used as substrates in rhodium-catalyzed asymmetric hydrogenation applying a mixed ligand system of monodentate phosphoramidites and phosphines. Optimization of the catalyst structure was achieved by high throughput experimentation. High enantioselectivities were obtained (up to 91%) with full conversion for a number of β-amino acids.

Graphical abstract: Enantioselective synthesis of β2-amino acids using rhodium-catalyzed hydrogenation

Article information

Article type
Paper
Submitted
18 Oct 2006
Accepted
20 Nov 2006
First published
08 Dec 2006

Org. Biomol. Chem., 2007,5, 267-275

Enantioselective synthesis of β2-amino acids using rhodium-catalyzed hydrogenation

R. Hoen, T. Tiemersma-Wegman, B. Procuranti, L. Lefort, J. G. de Vries, A. J. Minnaard and B. L. Feringa, Org. Biomol. Chem., 2007, 5, 267 DOI: 10.1039/B615131K

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