Volume 24, Issue 14
Natural Products
Full Access

ChemInform Abstract: Expeditious and Stereocontrolled Preparation of 2-Azido-2-deoxy-β- D-glucopyranose Derivatives from D-Glucal.

D. TAILLER

D. TAILLER

Lab. Biochim. Struct., UFR-Fac. Sci., Univ. Orleans, 45067 Orleans, Fr.

Search for more papers by this author
J.-C. JACQUINET

J.-C. JACQUINET

Lab. Biochim. Struct., UFR-Fac. Sci., Univ. Orleans, 45067 Orleans, Fr.

Search for more papers by this author
A.-M. NOIROT

A.-M. NOIROT

Lab. Biochim. Struct., UFR-Fac. Sci., Univ. Orleans, 45067 Orleans, Fr.

Search for more papers by this author
J.-M. BEAU

J.-M. BEAU

Lab. Biochim. Struct., UFR-Fac. Sci., Univ. Orleans, 45067 Orleans, Fr.

Search for more papers by this author
First published: April 6, 1993

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The azide (II), prepared in 3 steps from D-glucal (I), is transformed into the alcohol (V) and the imidate (VI) by stereoselective reactions. The latter are useful building blocks in the synthesis of oligosaccharides such as the disaccharide (VII).

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.