| Title | Semisynthesis and biological evaluation of abietane-type diterpenes. Revision of the structure of rosmaquinone. | | Author(s) | Marrero JG, Moujir L, Andrés LS, Montaño NP, Araujo L, Luis JG | | Institution | Instituto Universitario de Bio-Organica "Antonio Gonzalez", Departamento de Quimica Organica, Universidad de La Laguna, Avenida Astrofisico Francisco Sanchez 2, 38206 La Laguna, Tenerife, Canary Islands, Spain. | | Source | J Nat Prod 2009 Aug; 72(8):1385-9. | | Abstract | The new aromatic diterpenes 7beta-O-benzylrosmanol (3), 7beta-O-benzyl-11,12-di-O-methylrosmanol (4), and 7alpha-thiophenylcarnosic acid (5) have been obtained by partial synthesis from carnosol (1), an abundant natural diterpene present in Salvia species. The structures of these compounds were established from their physical and spectroscopic data. The known diterpenes sagequinone methide A (6), 7beta-O-methylrosmanol (7), 7-O-methylrosmanol (8), and rosmaquinone B (9) were obtained from rosmanol (2). The spectroscopic data of these semisynthetic diterpenes were identical to data reported in the literature. In addition, the new semisynthetic isorosmaquinone (10) was obtained from isorosmanol (12). The proton resonances of rosmaquinone (11) are reassigned based on 2D NMR spectroscopy. These compounds, as well as eight known analogues, were evaluated for cytotoxic and antimicrobial activities. | | Language | eng | | Pub Type(s) | Journal Article
Research Support, Non-U.S. Gov't
| | PubMed ID | 19711987 |
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