Computational Studies of the Arabinofuranose Ring: Conformational Preferences of Fully Relaxed Methyl α-d-arabinofuranoside
Author:
Affiliation:
1. Department of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp004611p
Reference55 articles.
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3. Arabinofuranosyl Oligosaccharides from Mycobacteria: Synthesis and Effect of Glycosylation on Ring Conformation and Hydroxymethyl Group Rotamer Populations
4. THE ENVELOPE OF MYCOBACTERIA
5. (a) Garrett, E. C.; Serianni, A. S.In Computer Modeling of CarbohydrateMolecules; French, A. D., Brady, J. W., Eds.; ACS Symposium Series 430. American Chemical Society: Washington, DC, 1990; pp 91−119.
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