1H-NMR Studies on (6R)- and (6S)-deuterated (1–6)-linked disaccharides: assignment of the preferred rotamers about C5–C6 bond of (1–6)-disaccharides in solution-Reference-Cited by-同舟云学术

1H-NMR Studies on (6R)- and (6S)-deuterated (1–6)-linked disaccharides: assignment of the preferred rotamers about C5–C6 bond of (1–6)-disaccharides in solution

Published:1985-01 Issue:27 Volume:26 Page:3251-3254
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ohrui Hiroshi,Nishida Yoshihiro,Watanabe Masato,Hori Hiroshi,Meguro Hiroshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Haworth Memorial Lecture. Human blood groups and carbohydrate chemistry

2. Further justification for the exo-anomeric effect. Conformational analysis based on nuclear magnetic resonance spectroscopy of oligosaccharides

3. The Preferred Conformation of Oligosaccharides Derived from the Complex-Type Carbohydrate Portions of Glycoproteins

4. High-Resolution, 1H-Nuclear Magnetic Resonance Spectroscopy as a Tool in the Structural Analysis of Carbohydrates Related to Glycoproteins

5. Solution conformation of asparagine-linked oligosaccharides: .alpha.(1-2)-, .alpha.(1-3)-, .beta.(1-2)-, and .beta.(1-4)-linked units

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