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Journal ArticleOPEN ACCESS

Studies on the biosynthesis of antibiotics

Pure and Applied Chemistry (1989) 61(3) 485-488
DOI: 10.1351/pac198961030485
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Abstract

Studies with stable isotope-labeled precursors followed by NMR analysis of the resulting antibiotics have revealed the biosynthetic origin and mode of formation of the cyclohexanecarboxylic acid moiety in ansatrienin, the mC 7 N unit in ansatrienin and asukamycin, the 2-amino-3-hydroxycyclopent-2-enone moiety of asukamycin and reductiomycin, and the dihydrofuranylacrylic acid moiety of reductiomycin. © 1989 IUPAC

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APA

Floss, H. G., Casati, R., Cho, H., & Beale, J. M. (1989). Studies on the biosynthesis of antibiotics. Pure and Applied Chemistry, 61(3), 485–488. https://doi.org/10.1351/pac198961030485

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