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  Synthesis and absolute configuration of the c-12-terpenoid dehydrogeosmin from the flower scents of rebutia-marsoneri and dolichothele-sphaerica (cactaceae) - a new approach to bis-angularly substituted trans-decalins

Huber, U., Boland, W., Konig, W. A., & Gehrcke, B. (1993). Synthesis and absolute configuration of the c-12-terpenoid dehydrogeosmin from the flower scents of rebutia-marsoneri and dolichothele-sphaerica (cactaceae) - a new approach to bis-angularly substituted trans-decalins. Helvetica Chimica Acta, 76(5), 1949-1955.

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BOL329.pdf (Publisher version), 0B
 
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Huber, U., Author
Boland, W.1, Author           
Konig, W. A., Author
Gehrcke, B., Author
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 Abstract: Optically pure(+)-(4S,4aS,8aS)-1,2,3,4,4a,5,8,8a-octahydro-4,8a-dimethylnaphthalen-4a-ol ((+)-1; dehydrogeosmin) is released from flower heads of the two cactaceae Rebutia marsoneri and Dolichothele sphaerica. The absolute configuration of (+)-1 is iden

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 Dates: 1993
 Publication Status: Issued
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 Identifiers: Other: BOL329
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Title: Helvetica Chimica Acta
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Source Genre: Journal
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Pages: - Volume / Issue: 76 (5) Sequence Number: - Start / End Page: 1949 - 1955 Identifier: -