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Acta Pharmaceutica Sinica ; (12): 364-366, 2012.
Article in English | WPRIM | ID: wpr-323035

ABSTRACT

One new sesquiterpene was isolated from the fermentation broth of Streptomyces sp. and the structure was elucidated by spectral analysis as caryolane-1, 6beta-diol (1). An intermediate 1alpha, 6beta, 11-eudesmanetriol (2) in the biosynthesis of geosmin was also found in this strain which proved sequence for the reactions, especially bicyclization preceding dealkylation.


Subject(s)
Magnetic Resonance Spectroscopy , Molecular Structure , Naphthols , Chemistry , Sesquiterpenes , Chemistry , Streptomyces , Chemistry
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