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Authordc.contributor.authorSaitz Barría, Claudio 
Authordc.contributor.authorCanete, Alvaro 
Authordc.contributor.authorMarquez, Amelia 
Authordc.contributor.authorRodriguez, L. M. H. 
Admission datedc.date.accessioned2018-12-20T15:04:11Z
Available datedc.date.available2018-12-20T15:04:11Z
Publication datedc.date.issued1996
Cita de ítemdc.identifier.citationBoletin de la Sociedad Chilena de Quimica, Volumen 41, Issue 3, 2018, Pages 295-299
Identifierdc.identifier.issn03661644
Identifierdc.identifier.urihttp://repositorio.uchile.cl/handle/2250/157474
Abstractdc.description.abstractThe azomethin ylide of the 2-p-methoxyphenyl-4-phenyl-2-oxazolin-5-one underwent 1,3-dipolar cycloaddition to both tautomers of the 1-nitroso-2-naphthol. The reaction yields two naphthoxazoles: 2-phenylnaphtho[1,2-d]oxazole, 2-p-methoxyphenylnaphtho[1,2-d]oxazole and a naphthoxazinone: 2-phenyl-3H-naphtho[2,1-b]-1,4-oxazin-3-one in approximately equal yields. Mechanisms for the formation of these compounds are proposed. The reaction provides a new synthesis of naphthoxazoles.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceBoletin de la Sociedad Chilena de Quimica
Keywordsdc.subjectChemistry (all)
Títulodc.titleReaccion entre el dipolo-1,3 enmascarado de una oxazolinonay 1-nitroso-2-naftol. Nueva sintesis de naftoxazoles
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile