Microbial hydroxylation/functionalization of terpenoid synthons derived from communic acids

Gérard Aranda (1) , R. Azerad (2) , M. Maurs (2) , G. Bertho (2) , D. Jiménez-González (3) , E. Cabrera-Torres (3) , A.F. Barrero (3)

1 DCSO - Laboratoire de synthèse organique
2 LCBPT - UMR 8601 - Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques
3 Departamento de Quı́mica Orgánica

Incubation of a communic acid-derived synthon with Cunninghamella elegans quantitatively affords 1ß, 3ß- and 7ß-monohydroxylated derivatives. (C) 2000 Elsevier Science Ltd.

Gérard Aranda, R. Azerad, M. Maurs, G. Bertho, D. Jiménez-González, et al.. Microbial hydroxylation/functionalization of terpenoid synthons derived from communic acids. Phytochemistry, 2000, 54 (1), pp.23-27. ⟨10.1016/s0031-9422(00)00032-7⟩. ⟨hal-00954903⟩