The Relative and Absolute Stereochemistry of the Antifungal Agent Preussin

The Journal of Antibiotics

Volumn 42, Issue 7, 1989, Pages 1184-1185

  Johnson, Janice H ^a   Phillipson, D W ^a   Kahle, Alicia D ^a  

^a Squibb Inst for Medical Research   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PREUSSIN;

ANTIFUNGAL ACTIVITY; DRUG STRUCTURE; FUNGUS; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; PRELIMINARY COMMUNICATION; PRIORITY JOURNAL; STEREOCHEMISTRY;

ANISOMYCIN; ANTIBIOTICS, ANTIFUNGAL; ASCOMYCOTA; CANDIDA; CHROMATOGRAPHY, THIN LAYER; FERMENTATION; FUNGI; ISOMERISM; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; PYRROLIDINES;

EID: 0024342172     PISSN: 00218820     EISSN: 18811469     Source Type: Journal    
DOI: 10.7164/antibiotics.42.1184     Document Type: Article

References (2)

1. Schwartz, R. E.; J. Liesch, O. Hensens, L. Zitano, S. Honeycutt, G. Garrity, R. A. Fromtling, J. Onishi & R. Monaghan: L-657, 398, a novel antifungal agent: Fermentation, isolation, structural elucidation and biological properties. J. Antibiotics 41: 1774~ 1779, 1988
2. Trost, B. M.; J. Belletire, S. Godleski, P. Mcdougal, J. Balkovec, J. Baldwin, M. Christy, G. Ponticello, S. Varga & J. Springer: On the use of the O-methylman-delate ester for establishment of absolute configuration of secondary alcohols. J. Org. Chem. 51: 2370–2374, 1986