Formation, and stereochemistry, of 1,2-O-(1-methyl-1,2-ethanediyl)-d-glucose acetals formed in the acid-catalyzed hydrolysis of O-(2-hydroxypropyl)cellulose
- 1 March 1984
- journal article
- Published by Elsevier in Carbohydrate Research
- Vol. 126 (1) , 101-114
- https://doi.org/10.1016/0008-6215(84)85129-0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Acid-catalyzed conversion of 2-O-(2-hydroxypropyl)-d-glucose derivatives into 1,2-O-(1-methyl-1,2-ethanediyl)-d-glucose acetals. Studies related to O-(2-hydroxypropyl)celluloseCarbohydrate Research, 1984
- Use of methanolysis in the characterization of O-(2-hydroxypropyl)cellulose by 13C-n.m.r. spectroscopyCarbohydrate Research, 1983
- 13C-N.M.R.-spectral and related studies on the distribution of substituents in O-(2-hydroxypropyl)celluloseCarbohydrate Research, 1982
- Lactol ring-opening in the solvolysis of a glycoside. Neighboring-group participation by 2-O-(2-hydroxyethyl) and 2-O-(2-hydroxypropyl) substituentsCarbohydrate Research, 1981
- Stereoelectronic control in acetal formationCanadian Journal of Chemistry, 1980
- Removal of O-benzyl protecting-groups of carbohydrate derivatives by catalytic, transfer hydrogenationCarbohydrate Research, 1980
- Deuterium-induced differential isotope shift carbon-13 NMR. 1. Resonance reassignments of mono- and disaccharidesJournal of the American Chemical Society, 1979
- Intramolecular acetal formation by primary versus secondary hydroxyl groupsCarbohydrate Research, 1978
- Carbon-13 Chemical Shifts of Furanosides and Cyclopentanols. Configurational and Conformational InfluencesCanadian Journal of Chemistry, 1975
- Stereoelectronic control in the cleavage of tetrahedral intermediates in the hydrolysis of esters and amidesTetrahedron, 1975