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J Org Chem ; 72(2): 643-6, 2007 Jan 19.
Article in English | MEDLINE | ID: mdl-17221988

ABSTRACT

Two chromatographically inseparable, diastereomeric eudesmane cyclic sulfites have been semisynthesized from alpha-santonin. This diastereomeric mixture was resolved by enzymatic acetylation with CCL. Each cyclic sulfite derivative was individually characterized on the basis of its spectroscopic and crystallographic properties.


Subject(s)
Lipase/chemistry , Sesquiterpenes, Eudesmane , Sulfites , Candida/enzymology , Crystallography, X-Ray , Cyclization , Magnetic Resonance Spectroscopy/methods , Magnetic Resonance Spectroscopy/standards , Models, Molecular , Reference Standards , Sensitivity and Specificity , Sesquiterpenes, Eudesmane/chemical synthesis , Sesquiterpenes, Eudesmane/chemistry , Stereoisomerism , Sulfites/chemical synthesis , Sulfites/chemistry
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