1H-NMR studies of (6r)- and (6s)-deuterated d-hexoses: assignment of the preferred rotamers about C5C6 bond of D-glucose and D-galactose derivatives in solutions-Reference-Cited by-同舟云学术

1H-NMR studies of (6r)- and (6s)-deuterated d-hexoses: assignment of the preferred rotamers about C5C6 bond of D-glucose and D-galactose derivatives in solutions

Published:1984-01 Issue:15 Volume:25 Page:1575-1578
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Nishida Yoshihiro,Ohrui Hiroshi,Meguro Hiroshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Molecular Rotations of Glucides in Relation to their Structures. IV. The Internal Conformation of C6–O Bond in D-Mannopyranose and D-Glucopyranose in their Aqueous Solutions

2. Molecular Rotations of Glucides in Relation to their Structures. V. The Internal Conformation ofC6–OBond in D-Galactopyranose in the Aqueous Solution and the Direction of the Optical Axis of Methylol Group

3. Studies of specifically fluorinated carbohydrates. Part I. Nuclear magnetic resonance studies of hexopyranosyl fluoride derivatives

4. Applications of empirical rules for optical rotation to problems of conformational analysis

5. Orientational Dependance of Vicinal and Geminal 13C–1H Coupling

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