Issue 5, 2004
From the journal:

Chemical Communications

Tandem aminoxylation–allylation reactions: a rapid, asymmetric conversion of aldehydes to mono-substituted 1,2-diols†

Guofu Zhong*a  

* Corresponding authors

a The Skaggs Institute for Chemical Biology and The Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA
E-mail: gzhong@scripps.edu
Fax: +1 858 784 2584
Tel: +1 858 784 9283

Abstract

A facile and rapid synthesis of enantiopure mono-substituted 1,2-diols was achieved by the tandem aminoxylation–allylation reactions of aldehydes.

Graphical abstract: Tandem aminoxylation–allylation reactions: a rapid, asymmetric conversion of aldehydes to mono-substituted 1,2-diols

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Article information

DOI
https://doi.org/10.1039/B314356B
Article type
Communication
Submitted
10 Nov 2003
Accepted
08 Jan 2004
First published
27 Jan 2004

Chem. Commun., 2004, 606-607

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Tandem aminoxylation–allylation reactions: a rapid, asymmetric conversion of aldehydes to mono-substituted 1,2-diols

G. Zhong, Chem. Commun., 2004, 606 DOI: 10.1039/B314356B

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