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
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference9 articles.
1. Molecular Rotations of Glucides in Relation to their Structures. II. The Conformation and the Absolute Configuration of Aldopyranoses-Physical Meaning of Hudson’s Isorotation Rule
2. Molecular Rotations of Glucides in Relation to their Structures. I. The Absolute Configuration of γ-Lactones
3. Molecular Rotations of Glucides in Relation to their Structures. III. Optical Superposition in Pentoses
4. 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
5. Representation of simple molecules by molecular orbitals
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1. Optical Rotation, Electronic Circular Dichroism, and Vibrational Circular Dichroism of Carbohydrates and Glycoconjugates;Comprehensive Chiroptical Spectroscopy;2012-02-17
2. Empirical relationship between structure and molecular optical rotation in tetrahydropyran derivatives;Journal of Molecular Structure;1998-02
3. The preferred rotamer about the C5—C6 bond of D-galactopyranoses and the stereochemistry of dehydrogenation by D-galactose oxidase;Canadian Journal of Chemistry;1987-06-01
4. 1H-NMR studies of (6r)- and (6s)-deuterated d-hexoses: assignment of the preferred rotamers about C5C6 bond of D-glucose and D-galactose derivatives in solutions;Tetrahedron Letters;1984-01
5. Applications of empirical rules for optical rotation to problems of conformational analysis;Carbohydrate Research;1970-04
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