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Authordc.contributor.authorPérez, Edwin G. 
Authordc.contributor.authorSáez, Jairo es_CL
Authordc.contributor.authorCassels Niven, Brucees_CL
Admission datedc.date.accessioned2007-04-19T14:58:03Z
Available datedc.date.available2007-04-19T14:58:03Z
Publication datedc.date.issued2005-09
Cita de ítemdc.identifier.citationJOURNAL OF THE CHILEAN CHEMICAL SOCIETY 50 (3): 553-557 SEP 2005en
Identifierdc.identifier.issn0717-9324
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/118577
Abstractdc.description.abstractThe leaves of Duguetia vallicola, a fairly common, large evergreen tree from the coastal regions of Panama, Colombia and Venezuela, contain (6aS)-glaziovine (1) as a major constituent. The abundance and renewable character of the plant material make it an attractive source for this rare, psychoactive alkaloid. The availability of glaziovine and its 0-methyl derivative pronuciferine (2) has made complete H-1 and C-13 NMR assignments of proaporphines possible for the first time.en
Lenguagedc.language.isoenen
Publisherdc.publisherSOCIEDAD CHILENA DE QUIMICAen
Keywordsdc.subjectISOQUINOLINE ALKALOIDSen
Títulodc.titleA convenient, renewable source of the anxiolytic proaporphine alkaloid glaziovine: Duguetia vallicola leavesen
Document typedc.typeArtículo de revista


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