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
- 1 August 1957
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 30 (8) , 920-924
- https://doi.org/10.1246/bcsj.30.920
Abstract
The internal conformation of C6–O bond in the molecules of d-mannopyranose and d-glucopyranose in aqueous solutions were presumed by a new method, and was concluded to take trans (mostly) and gauche II (only sometimes) forms.This publication has 6 references indexed in Scilit:
- Molecular Rotations of Glucides in Relation to their Structures. III. Optical Superposition in PentosesBulletin of the Chemical Society of Japan, 1957
- Molecular Rotations of Glucides in Relation to their Structures. II. The Conformation and the Absolute Configuration of Aldopyranoses-Physical Meaning of Hudson’s Isorotation RuleBulletin of the Chemical Society of Japan, 1957
- The crystal and molecular structure of α-glucoseActa Crystallographica, 1952
- The Absolute Configuration of Optically Active MoleculesThe Journal of Chemical Physics, 1952
- On the Theory of Optical Rotatory PowerThe Journal of Chemical Physics, 1937
- Two Forms of Anhydrous l-Rhamnose and a New Method for the Preparation of Crystalline β-Tetraacetyl-l-rhamnose1Journal of the American Chemical Society, 1937