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Is phototridachiahydropyrone a true natural product?
Gavagnin, Margherita; Mollo, Ernesto; Cimino, Guido.
  • Gavagnin, Margherita; Istituto di Chimica Biomolecolare. Consiglio Nazionale delle Ricerche. Pozzuoli. IT
  • Mollo, Ernesto; Istituto di Chimica Biomolecolare. Consiglio Nazionale delle Ricerche. Pozzuoli. IT
  • Cimino, Guido; Istituto di Chimica Biomolecolare. Consiglio Nazionale delle Ricerche. Pozzuoli. IT
Rev. bras. farmacogn ; 25(6): 588-591, Nov.-Dec. 2015. tab, graf
Artículo en Inglés | LILACS | ID: lil-769951
ABSTRACT
Abstract The occurrence of (−)-phototridachiahydropyrone (5) in nature has been proven. This compound has been now identified as minor component of the extract of marine sacoglossan mollusk Elysia crispata from which the main (−)-tridachiahydropyrone (4) was previously described. Synthetic (±)-5 was formerly obtained by Moses’ group by biomimetic photochemical conversion of (±)-tridachiahydropyrone (4). The same authors suggested that compound 5 had to be a natural product derived from precursor 4 “yet to be discovered”. Comparison of CD profiles of natural (−)-4 and (−)-5 indicated the same absolute configuration for both compounds. This evidence is in agreement with the concerted mechanism proposed for the photochemical conversion.


Texto completo: Disponible Índice: LILACS (Américas) Idioma: Inglés Revista: Rev. bras. farmacogn Asunto de la revista: Farmacia Año: 2015 Tipo del documento: Artículo País de afiliación: Italia Institución/País de afiliación: Istituto di Chimica Biomolecolare/IT

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Texto completo: Disponible Índice: LILACS (Américas) Idioma: Inglés Revista: Rev. bras. farmacogn Asunto de la revista: Farmacia Año: 2015 Tipo del documento: Artículo País de afiliación: Italia Institución/País de afiliación: Istituto di Chimica Biomolecolare/IT