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Gris, A.; Cabedo Escrig, N.; Navarro Fuertes, I.; De Alfonso, I.; Agullo, C.; Abad Somovilla, A. (2012). General Diastereoselective Synthetic Approach toward Isospongian Diterpenes. Synthesis of (-)-Marginatafuran, (-)-Marginatone, and (-)-20-Acetoxymarginatone. Journal of Organic Chemistry. 77(13):5664-5680. doi:10.1021/jo3008034
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/70128
Título: | General Diastereoselective Synthetic Approach toward Isospongian Diterpenes. Synthesis of (-)-Marginatafuran, (-)-Marginatone, and (-)-20-Acetoxymarginatone | |
Autor: | Gris, A. Cabedo Escrig, Nuria Navarro Fuertes, Ismael de Alfonso, I. Agullo, C. Abad Somovilla, Antonio | |
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This work describes a synthetic approach to the carbocyclic skeleton of isospongian diterpenes that uses the commercially available monoterpene (S)-carvone as a C-ring synthon, which is incorporated into the tetracyclic ...[+]
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Derechos de uso: | Cerrado | |
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Versión del editor: | http://dx.doi.org/10.1021/jo3008034 | |
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We thank the Spanish Ministerio de Ciencia e Innovacion (MICINN) and the company EPA S.L. (Cadet, Spain) for their continuous support of our work (Projects BQU2002-00272 and AGL2009-12940-C02-02). We also thank the S.C.S.I.E. ...[+]
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