Formation, Structure, and Synthetic Use of Gluco- and Galactopyranoside Acetophenone Acetals with 1,3-Dioxane Rings
- 1 March 1983
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 22 (3) , 255-256
- https://doi.org/10.1002/anie.198302551
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- p-Methoxyacetophenone dimethyl ketal and .alpha.,p-dimethoxystyrene. Efficient and useful reagents for 1,2- and 1,3-diol protectionThe Journal of Organic Chemistry, 1981
- Preparation and N.M.R. studies of pyruvic acid and related acetals of pyranosides: configuration at the acetal carbon atomsCarbohydrate Research, 1979
- Calorimetric determination of the conformational enthalpy and entropy of 2-phenyl-1,3-dioxane. Effectively free rotation of an equatorial 2-phenyl group. Conformational equilibriums in 2,2-disubstituted 1,3-dioxanesJournal of the American Chemical Society, 1978
- Stereoselective hydrogenolysis of exo- and endo-2,3-benzylidene acetals of hexopyranosidesCarbohydrate Research, 1976
- Acetal exchange reactionsCarbohydrate Research, 1967
- Diastereoisomeric forms of methyl 4,6-O-benzylidene-2,3-di-O-methyl-α-d-gluco- and α- and β-d-galactopyranosideCarbohydrate Research, 1965