Abstract
The structures of novel macrolide antibiotics, quinolidomicins Al5 A2and Bls were elucidated as shown in Fig. 1 by NMRspectral analysis including a variety of two-dimensional techniques. The quinolidomicins possess a novel 60-memberedmacrolide ring, which is to our knowledge the largest amongnatural products. © 1993, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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CITATION STYLE
Yoichi, H., Kazuo, S., Kazuo, F., & Haruo, S. (1993). Quinolidomicins a1, a2 and b1, novel 60-membered macrolide antibiotics II. Structureelucidation. The Journal of Antibiotics, 46(10), 1563–1569. https://doi.org/10.7164/antibiotics.46.1563
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