Aplysiols A and B, squalene-derived polyethers from the mantle of the sea hare Aplysia dactylomela. (Articolo in rivista)

Type
Label
  • Aplysiols A and B, squalene-derived polyethers from the mantle of the sea hare Aplysia dactylomela. (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tet.2007.07.055 (literal)
Alternative label
  • E. Manzo; M. Gavagnin; G. Bifulco; P. Cimino; S. Di Micco; M. L. Ciavatta; Y.-W. Guo; G. Cimino. (2007)
    Aplysiols A and B, squalene-derived polyethers from the mantle of the sea hare Aplysia dactylomela.
    in Tetrahedron (Oxf., Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • E. Manzo; M. Gavagnin; G. Bifulco; P. Cimino; S. Di Micco; M. L. Ciavatta; Y.-W. Guo; G. Cimino. (literal)
Pagina inizio
  • 9970 (literal)
Pagina fine
  • 9978 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 63 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 40 (literal)
Note
  • Scopu (literal)
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di Chimica Biomolecolare, CNR, Via Campi Flegrei 34, 80078 Pozzuoli, Naples, Italy Dipartimento di Scienze Farmaceutiche, Universita' di Salerno, Via Ponte Don Melillo, 84084 Fisciano, Salerno, Italy State Key Laboratory of Drug Research, Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 201203 Shanghai, China (literal)
Titolo
  • Aplysiols A and B, squalene-derived polyethers from the mantle of the sea hare Aplysia dactylomela. (literal)
Abstract
  • Two novel triterpenoids, aplysiols A (5) and B (6), have been isolated, together with structurally related known metabolites, from a South China Sea collection of the anaspidean mollusc Aplysia dactylomela. The structures of 5 and 6 were determined mainly by spectroscopic NMR techniques. The absolute stereochemistry of compound 5 was deduced by Mosher's method as well as by biogenetical consideration, whereas the absolute stereochemistry of compound 6 was established also using an integrated NMR-QM (Quantum Mechanical) approach, based on the combination of 13C NMR chemical shifts and 2,3JC-H coupling constant DFT (density functional theory) calculations. (literal)
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