Volume 29, Issue 1
Natural Products
Full Access

ChemInform Abstract: Stereoselective Addition of 2-Furyllithium and 2-Thiazolyllithium to Sugar Nitrones. Synthesis of Carbon-Linked Glycoglycines.

A. DONDONI

A. DONDONI

Lab. Chim. Org., Dip. Chim., Univ. Ferrara, I-44100 Ferrara, Italy

Search for more papers by this author
F. JUNQUERA

F. JUNQUERA

Lab. Chim. Org., Dip. Chim., Univ. Ferrara, I-44100 Ferrara, Italy

Search for more papers by this author
F. L. MERCHAN

F. L. MERCHAN

Lab. Chim. Org., Dip. Chim., Univ. Ferrara, I-44100 Ferrara, Italy

Search for more papers by this author
P. MERINO

P. MERINO

Lab. Chim. Org., Dip. Chim., Univ. Ferrara, I-44100 Ferrara, Italy

Search for more papers by this author
M.-C. SCHERRMANN

M.-C. SCHERRMANN

Lab. Chim. Org., Dip. Chim., Univ. Ferrara, I-44100 Ferrara, Italy

Search for more papers by this author
T. TEJERO

T. TEJERO

Lab. Chim. Org., Dip. Chim., Univ. Ferrara, I-44100 Ferrara, Italy

Search for more papers by this author
First published: 24 June 2010

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 and quite general route to sugar glycines in both epimeric forms is reported based on stereoselective addition of the lithium compounds (II) and (XII) to the sugar nitrones (I) and (XI). Opposite diastereofacial selectivity is observed depending on the presence or absence of Et2AlCl.

chemical structure image

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