» Articles » PMID: 6704994

2-Bromoethyl Glycosides in Glycoside Synthesis: Preparation of Glycoproteins Containing Alpha-L-Fuc-(1----2)-D-Gal and Beta-D-Gal-(1----4)-D-GlcNAc

Overview
Journal Carbohydr Res
Publisher Elsevier
Date 1984 Feb 15
PMID 6704994
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

The applicability of 2-bromoethyl glycosides in carbohydrate synthesis is demonstrated by the synthesis of glycosides of alpha-L-Fuc-(1----2)-D-Gal and beta-D-Gal-(1----4)-D-GlcNAc. The bromoethyl aglycon was transformed into the methoxycarbonylethylthioethyl spacer, which allowed coupling of the sugars to proteins (BSA and KLH).

Citing Articles

Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2.

Wang T, Nigudkar S, Yasomanee J, Rath N, Stine K, Demchenko A Org Biomol Chem. 2018; 16(19):3596-3604.

PMID: 29693690 PMC: 5971085. DOI: 10.1039/c8ob00477c.


The PapG adhesin of uropathogenic Escherichia coli contains separate regions for receptor binding and for the incorporation into the pilus.

Hultgren S, Lindberg F, Magnusson G, Kihlberg J, Tennent J, Normark S Proc Natl Acad Sci U S A. 1989; 86(12):4357-61.

PMID: 2567514 PMC: 287268. DOI: 10.1073/pnas.86.12.4357.