Alkaline and enzymatic hydrolysis of isobutyl 3,4-anhydro-2,6-dideoxy-DL-hexopyranosides. Preparation of enantiomeric boivinopyranosides through a highly efficient kinetic resolution

Alkaline and enzymatic hydrolysis of isobutyl 3,4-anhydro-2,6-dideoxy-DL-hexopyranosides. Preparation of enantiomeric boivinopyranosides through a highly efficient kinetic resolution

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Bibliographic Details
Published in:Journal of organic chemistry Vol. 52; no. 13; pp. 2886 - 2892
Main Authors: Barili, Pier Luigi, Berti, Giancarlo, Catelani, Giorgio, Colonna, Fabrizia, Mastrorilli, Ettore
Format: Journal Article
Language:English
Published: Washington, DC American Chemical Society 01-06-1987
Subjects:
Bioconversions. Hemisynthesis
Biological and medical sciences
Biotechnology
Carbohydrates with 4, 5, 6, ... C atoms, dissacharides and oligosaccharides
Carbohydrates. Nucleosides and nucleotides
Chemistry
Exact sciences and technology
Fundamental and applied biological sciences. Psychology
Methods. Procedures. Technologies
Organic chemistry
Preparations and properties
Hydrolysis
Glycoside
NMR spectrum
Epoxide hydrolase
Base reaction
Hemisynthesis
Enzymatic reaction
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Description
Bibliography:istex:4C367C67CAACD1F6D969D8DABFEB94E10747F2E2
ark:/67375/TPS-Q26SFVGR-4
ISSN:0022-3263
1520-6904
DOI:10.1021/jo00389a042