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Synthesis of (+)-Hanagokenol A, (+)-Fortunins E, G, H, and (-)-Sugikurojin A from Abietic Acid
Abstract A series of 12-hydroxy-substituted abietane diterpenes, functionalized on C19 or C18, have been synthesized starting from 18-hydroxyferruginol. The first synthesis of antibacterial hanagokenol A and fortunins E, G, and H, and a new procedure for preparing sugikurojin A and the immunosuppres...
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Published in: | Synthesis (Stuttgart) 2010-10, Vol.2010 (20), p.3493-3503 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
A series of 12-hydroxy-substituted abietane diterpenes, functionalized
on C19 or C18, have been synthesized starting from 18-hydroxyferruginol.
The first synthesis of antibacterial hanagokenol A and fortunins
E, G, and H, and a new procedure for preparing sugikurojin A and
the immunosuppressive 19-hydroxyÂ-ferruginol are reported. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-0030-1258226 |