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Authordc.contributor.authorAlmodovar, Iriux 
Authordc.contributor.authorCardona, Wilson es_CL
Authordc.contributor.authorDelgado Castro, Tomás es_CL
Authordc.contributor.authorZapata Torres, Gerald Amilcar es_CL
Authordc.contributor.authorCaroli Rezende, Marcos es_CL
Authordc.contributor.authorAraya Maturana, Ramiro es_CL
Authordc.contributor.authorMaestro, M. Carmen es_CL
Authordc.contributor.authorGarcía Ruano, José L. es_CL
Admission datedc.date.accessioned2014-03-12T20:36:14Z
Available datedc.date.available2014-03-12T20:36:14Z
Publication datedc.date.issued2013
Cita de ítemdc.identifier.citationTetrahedron: Asymmetry 24 (2013) 56–61en_US
Identifierdc.identifier.otherdoi10.1016/j.tetasy.2012.11.017
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121855
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractDiels–Alder cycloaddition of 8,8-dimethylnaphthalene-1,4,5(8H)-trione with diastereomeric hydroxysulfinyldienes proceeded with high yields and good p-facial and regioselectivities. The hydroxysulfoxide moiety controls the regio- and stereoselectivities, through hydrogen bonds in the suggested transition state.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevieren_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Títulodc.titleRemote regio- and stereocontrol by the sulfinyl group: Diels–Alder reaction of sulfinyl dienols and 8,8-dimethylnaphthalene-1,4,5(8H)-trioneen_US
Document typedc.typeArtículo de revista


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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