Issue 21, 2003

Highly stereoselective synthesis of (−)-monatin, a high-intensity sweetener, using chelation-controlled nitrone cycloaddition

Abstract

Synthesis of (−)-monatin was achieved by chelation-controlled cycloaddition of nitrone 2 with allyl alcohol 3a in the presence of MgBr2·OEt2.

Graphical abstract: Highly stereoselective synthesis of (−)-monatin, a high-intensity sweetener, using chelation-controlled nitrone cycloaddition

Supplementary files

Article information

Article type
Communication
Submitted
13 Jun 2003
Accepted
04 Sep 2003
First published
24 Sep 2003

Chem. Commun., 2003, 2678-2679

Highly stereoselective synthesis of (−)-monatin, a high-intensity sweetener, using chelation-controlled nitrone cycloaddition

O. Tamura, T. Shiro, A. Toyao and H. Ishibashi, Chem. Commun., 2003, 2678 DOI: 10.1039/B306791M

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