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  • Title: Structural studies on lipiarmycin. I. Characterization by 1H and 13C NMR spectroscopy and isolation of methyl 2-O-methyl-4-O-homodichloroorsellinate-beta-rhamnoside.
    Author: Martinelli E, Faniuolo L, Tuan G, Gallo GG, Cavalleri B.
    Journal: J Antibiot (Tokyo); 1983 Oct; 36(10):1312-22. PubMed ID: 6643280.
    Abstract:
    1H and 13C NMR spectral studies of lipiarmycin in CDCl3 and in pyridine-d5 provided evidence for the six partial structures I approximately VI and the two sugar units 1 and 2. Acid methanolysis led to the isolation of methyl 2-O-methyl-4-O-homodichloroorsellinate-beta-rhamnoside, whose structure was determined by spectroscopic methods.
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