Volume 28, Issue 50
Natural Products
Full Access

ChemInform Abstract: Direct Glycosylations with 1-Hydroxy Glycosyl Donors Using Trifluoromethanesulfonic Anhydride and Diphenyl Sulfoxide.

B. A. GARCIA

B. A. GARCIA

Dep. Chem., Univ. Ill., Urbana, IL 61801, USA

Search for more papers by this author
J. L. POOLE

J. L. POOLE

Dep. Chem., Univ. Ill., Urbana, IL 61801, USA

Search for more papers by this author
D. Y. GIN

D. Y. GIN

Dep. Chem., Univ. Ill., Urbana, IL 61801, USA

Search for more papers by this author
First published: 02 August 2010
Citations: 1

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

A new method for glycosidic bond construction is described involving in situ activation of the anomeric hydroxyl. This one-step procedure is applicable directly to the glycosylation of a wide range of acceptors. The C-2 neighboring group effects the glycosylation stereochemistry. In the case of (XII) β-selectivity is observed exclusively.

chemical structure image

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