Structural studies on lipiarmycin I. Characterization by 1H and 13C NMR spectroscopy and isolation of methyl 2-O-methyl-4-O-homodichloroorsellinate-.BETA.-rhamnoside.
- 1 January 1983
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 36 (10) , 1312-1322
- https://doi.org/10.7164/antibiotics.36.1312
Abstract
1H and 13C NMR spectral studies of lipiarmycin in 3H-labeled CHCl3 and pyridine-d5 provided evidence for the 6 partial structures and the 2 sugar units. Acid methanolysis led to the isolation of methyl 2-O-methyl-4-O-homodichloroorsellinate-.beta.-rhamnoside, whose structure was determined by spectroscopic methods.This publication has 0 references indexed in Scilit: