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The regioselective bromination of 4,4-dimethyl-5,8-dihydroxy-4H- naphthalen-1-one

Authordc.contributor.authorMejias, Lorenzo 
Authordc.contributor.authorSepúlveda, Silvia 
Authordc.contributor.authorAraya Maturana, Ramiro 
Authordc.contributor.authorCassels Niven, Bruce 
Authordc.contributor.authorRezende, Marcos Caroli 
Admission datedc.date.accessioned2018-12-20T14:06:43Z
Available datedc.date.available2018-12-20T14:06:43Z
Publication datedc.date.issued1998
Cita de ítemdc.identifier.citationSynthetic Communications, Volumen 28, Issue 23, 2018, Pages 4365-4370
Identifierdc.identifier.issn00397911
Identifierdc.identifier.other10.1080/00397919808004471
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/153964
Abstractdc.description.abstractMethods for the regioselective bromination of the title naphthalenone are described, which lead to isomeric hydroquinones 5 or 6.
Lenguagedc.language.isoen
Publisherdc.publisherMarcel Dekker Inc.
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceSynthetic Communications
Keywordsdc.subjectOrganic Chemistry
Títulodc.titleThe regioselective bromination of 4,4-dimethyl-5,8-dihydroxy-4H- naphthalen-1-one
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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