Examination of the influence of C5-hydroxymethyl group and configurations of hydroxyl groups at C2, C3, and C4 stereocentres on the N-glycosidic torsion: synthesis and X-ray crystallographic investigation of N-(d-ribopyranosyl)alkanamides as N-glycoprotein linkage region analogs-Reference-Cited by-同舟云学术

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Examination of the influence of C5-hydroxymethyl group and configurations of hydroxyl groups at C2, C3, and C4 stereocentres on the N-glycosidic torsion: synthesis and X-ray crystallographic investigation of N-(d-ribopyranosyl)alkanamides as N-glycoprotein linkage region analogs

Published:2014-01 Issue: Volume:384 Page:37-45
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Srivastava Amrita,Mathiselvam Manoharan,Varghese Babu,Loganathan Duraikkannu

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference20 articles.

1. Glycobiology: Toward Understanding the Function of Sugars

2. Biological roles of oligosaccharides: all of the theories are correct

3. Intracellular Functions of N-Linked Glycans

4. On the structural significance of the linkage region constituents of N-glycoproteins: an X-ray crystallographic investigation using models and analogs

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