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(4bS,8aS)-1-Isopropyl-4b,8,8-trimethyl-4b,5,6,7,8,8a,9,10-octa­hydro­phenan­thren-2-yl benzoate

The title compound, C(27)H(34)O(2), was hemisynthesized through direct benzoyl­ation of the naturally occurring meroterpene totarol. The central fused six-membered ring has a half-chair conformation, whereas the terminal six-membered ring displays a chair conformation. The dihedral angle between the...

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Detalles Bibliográficos
Autores principales: Oubabi, Radouane, Auhmani, Aziz, Ait Itto, My Youssef, Auhmani, Abdelwahed, Daran, Jean-Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158506/
https://www.ncbi.nlm.nih.gov/pubmed/25249914
http://dx.doi.org/10.1107/S1600536814015827
Descripción
Sumario:The title compound, C(27)H(34)O(2), was hemisynthesized through direct benzoyl­ation of the naturally occurring meroterpene totarol. The central fused six-membered ring has a half-chair conformation, whereas the terminal six-membered ring displays a chair conformation. The dihedral angle between the fused benzene ring and the benzoyl benzene ring is 73.05 (14)°. The S,S chirality of the mol­ecule is consistent with the synthetic pathway, and confirmed by the refinement of the Flack parameter.