TOTAL SYNTHESIS OF CLAVUKERIN-A AND ITS EPIMER

Enantioselective synthesis of clavukerin A and its epimer was carried out. By the comparison of the spectral data and specific rotations of synthesized and natural ones, two trisnorsesquiterpens isolated from Clavulia and Cespitularia species are confirmed to be identical.

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Bibliographic Details
Published inChemistry letters no. 8; pp. 1295 - 1298
Main Authors ASAOKA, M, KOSAKA, T, ITAHANA, H, TAKEI, H
Format Journal Article
LanguageEnglish
Published TOKYO Chemical Soc Japan 01.08.1991
Subjects
Chemistry
Chemistry, Multidisciplinary
Physical Sciences
Science & Technology
CORAL CLAVULARIA-KOELLIKERI
TRINOR-GUAIANE SESQUITERPENE
IODIDE
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Summary:Enantioselective synthesis of clavukerin A and its epimer was carried out. By the comparison of the spectral data and specific rotations of synthesized and natural ones, two trisnorsesquiterpens isolated from Clavulia and Cespitularia species are confirmed to be identical.
ISSN:0366-7022
1348-0715
DOI:10.1246/cl.1991.1295