Abstract
Fluvirucin A1 was established as (2R,3S,6R,10S)-3-[(3-amino-3,6-dideoxy-α-l-talopyranosyl)-oxy]-2,6-dimethyl-10-ethyl-13-tridecanelactam by chemical, spectroscopic, and X-ray crystallographic analyses. © 1991, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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CITATION STYLE
APA
Inouye, Y., Kakisawa, H., & Oki, T. (1991). Fluvirucins a1, A2, B1, B2, B3, B4 and B5, new antibiotics active against influenza a virus: III. the stereochemistry and absolute configuration of fluvirucin A1. The Journal of Antibiotics, 44(7), 756–761. https://doi.org/10.7164/antibiotics.44.756
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