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Rev Biol Trop ; 52(1): 269-85, 2004 Mar.
Artigo em Espanhol | MEDLINE | ID: mdl-17357425

RESUMO

The roots of Croton hirtus (Euphorbiaceae) collected in Paraiso, Cartago (Costa Rica) afforded, in addition to the few known metabolites, 20 new compounds: the bis-nor dolabradane 1, the dolabradanes 2 and 3, the kauranes 4-7, the cyclopropakauranes 8 and 9, the hirtusanes 10-15, the germacradiene esters 16-18 and the C-25 compound 21, presumably formed by a Diels-Alder reaction between compound 18 and a monoterpene. All structures were elucidated using high field 1D and 2D NMR techniques. MS fragmentation patterns are here reported. The absolute configurations of 4 and 9 were elucidated by using circular dichroism. The separation was performed with modern chromatographic technics.


Assuntos
Croton/química , Diterpenos/isolamento & purificação , Raízes de Plantas/química , Cromatografia Líquida de Alta Pressão , Diterpenos/química , Extratos Vegetais/química
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