Partial synthesis of some diterpenoids with potential antitumour activity
Abstract
The diterpenoid fungal metabolite, fujenal, has been converted into analogues of the Rabdosia diterpenoids, ent-7-hydroxy-15-oxo-6,7-secokaur-16-en-6,19-dioic acid 6,7-lactone 19-methyl ester and ent-7-acetoxy-19-hydroxy-15-oxo-6,7-secokaur-16-en-6-oic acid 6,19-lactone which possess moderate inhibitory activity against HeLa cells.
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