4.5 Article

Synthesis of (+)-Hanagokenol A, (+)-Fortunins E, G, H, and (-)-Sugikurojin A from Abietic Acid

Journal

SYNTHESIS-STUTTGART
Volume -, Issue 20, Pages 3493-3503

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0030-1258226

Keywords

antibiotics; diastereoselectivity; phenols; terpenoids; oxidation

Funding

  1. Regional Government of Andalucia [P07-FQM-03101, FQM-348]
  2. Spanish Agency for the International Development and Cooperation (AECID)

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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-hydroxyferruginol are reported.

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