Jump to main content
Jump to site search

Issue 1, 2001
Previous Article Next Article

Dynamic kinetic resolution of tert-butyl 4-methyl-3,5-dioxohexanoate through enzymatic reduction

Author affiliations

Abstract

An entirely new method for the dynamic kinetic resolution of a racemic, 2-methyl substituted, unsymmetrical 1,3-diketone via enzymatic reduction to give an enantiomerically pure compound is introduced.

Back to tab navigation

Article information


Submitted
08 Sep 2000
Accepted
15 Nov 2000
First published
14 Dec 2000

Chem. Commun., 2001, 57-58
Article type
Communication

Dynamic kinetic resolution of tert-butyl 4-methyl-3,5-dioxohexanoate through enzymatic reduction

A. Ji, M. Wolberg, W. Hummel, C. Wandrey and M. Müller, Chem. Commun., 2001, 57 DOI: 10.1039/B007448I

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

Search articles by author

Spotlight

Advertisements