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Authordc.contributor.authorSoto, R. 
Authordc.contributor.authorMeyer, G. 
Authordc.contributor.authorViout, P. 
Admission datedc.date.accessioned2018-12-20T14:05:47Z
Available datedc.date.available2018-12-20T14:05:47Z
Publication datedc.date.issued1981
Cita de ítemdc.identifier.citationTetrahedron, Volumen 37, Issue 17, 2018, Pages 2977-2982
Identifierdc.identifier.issn00404020
Identifierdc.identifier.other10.1016/S0040-4020(01)98910-0
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/153760
Abstractdc.description.abstractThe general acid catalysed hydrolysis and the intramolecular nucleophilic anionic cyclization of acyloximes operate concurrently in water at pH 7-9. Hydrolysis is inhibited by cationic micelles; changing the length of the acyl chain does not affect the micellar effect, possibly because the environment of the reacting species is not influenced by this variation in the structure of the micelle. © 1981.
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.sourceTetrahedron
Keywordsdc.subjectBiochemistry
Keywordsdc.subjectDrug Discovery
Keywordsdc.subjectOrganic Chemistry
Títulodc.titleCatalyse et inhibition de deux reactions concurrentes en milieu micellaire cationique
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