http://www.cnr.it/ontology/cnr/individuo/prodotto/ID15240
Structural and stereochemical revision of isocyanide and isothiocyanate amphilectenes from the Caribbean marine sponge Cribochalina sp. (Articolo in rivista)
- Type
- Label
- Structural and stereochemical revision of isocyanide and isothiocyanate amphilectenes from the Caribbean marine sponge Cribochalina sp. (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tet.2005.05.102 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Ciavatta M.L.; Gavagnin M.; Manzo E.; Puliti R.; Mattia C. A.; Mazzarella L.; Cimino G.; Simpson J.S.; Garson M.J. (literal)
- Pagina inizio
- Pagina fine
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- Rivista
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- Scopu (literal)
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Chimica Biomolecolare, C.N.R., 80078 Pozzuoli, Italy;
Dipartimento di Scienze Farmaceutiche, Universita` di Salerno, via Ponte Don Melillo, I-84084 Fisciano, Salerno, Italy;
Dipartimento di Chimica, Universita` \"Federico II\", Complesso Universitario di Monte S. Angelo, via Cintia, I-80126 Napoli, Italy;
Department of Medicinal Chemistry, Victorian College of Pharmacy, Monash University, 381 Royal Parade, Parkville Vic. 3052, Australia;
School of Molecular and Microbial Sciences, The University of Queensland, Brisbane Qld 4072, Australia (literal)
- Titolo
- Structural and stereochemical revision of isocyanide and isothiocyanate amphilectenes from the Caribbean marine sponge Cribochalina sp. (literal)
- Abstract
- The absolute stereochemistry of amphilectene metabolites from Cribochalina sp. has been revised by a detailed NMR
spectroscopic study of the Mosher ester derivatives of a related alcohol. The relative stereochemistry of the previously described
amphilectenes has been reinvestigated and reassigned on the basis of the X-ray structural analysis carried out on one of them. The structure of
a new amphilectene metabolite, which is an isothiocyanato analogue is also presented (literal)
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