Oxidation of methyl glycopyranosides by Acetobactersuboxydans
- 1 July 1978
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 56 (13) , 1752-1757
- https://doi.org/10.1139/v78-284
Abstract
A synthesis of methyl pentopyranosid-4-uloses bas been achieved by microbiological oxidation by Acetobacter suboxydans of some methyl pentopyranosides. The oxidation products were isolated as their O-methyloxime derivatives, and the assignment of the configuration of the oximes was made on the basis of the carbon-13 magnetic resonance spectra. An analysis of the oxidative specificity of A. suboxydans towards methyl glycopyranosides is presented.This publication has 4 references indexed in Scilit:
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- Cyclitol oxidation by Acetobacter suboxydans. II. Additional cyclitols and the “third specificity rule”Archives of Biochemistry and Biophysics, 1958