Bookmark
Forward
Structural studies on lipiarmycin. I. Characterization by 1H and 13C NMR spectroscopy and isolation of methyl 2-O-methyl-4-O-homodichloroorsellinate-beta-rhamnoside.
E Martinelli, L Faniuolo, G Tuan, G G Gallo, B Cavalleri
The Journal of antibiotics 1983 Oct
Sizes of these terms reflect their relevance to your search.
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.
Citation
E Martinelli, L Faniuolo, G Tuan, G G Gallo, B Cavalleri.
Structural studies on lipiarmycin. I. Characterization by 1H and 13C NMR spectroscopy and isolation of methyl 2-O-methyl-4-O-homodichloroorsellinate-beta-rhamnoside.
The Journal of antibiotics.
1983 Oct;36(10):1312-22
Mesh Tags
Aminoglycosides
Anti-Bacterial Agents
Chemical Phenomena
Chemistry
Glycosides
Hydrogen Bonding
Magnetic Resonance Spectroscopy
Mass Spectrometry
Spectrophotometry, Infrared
Substances
Aminoglycosides
Anti-Bacterial Agents
Glycosides
lipiarmycin
methyl 2-O-methyl-4-O-homodichloroorsellinate-beta-rhamnoside
PMID: 6643280
View Full Text