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Authordc.contributor.authorAlmodovar, Iriux 
Authordc.contributor.authorCardona, Wilson 
Authordc.contributor.authorDelgado Castro, Tomás 
Authordc.contributor.authorZapata Torres, Gerald 
Authordc.contributor.authorCaroli Rezende, Marcos 
Authordc.contributor.authorAraya Maturana, Ramiro 
Authordc.contributor.authorMaestro, M. Carmen 
Authordc.contributor.authorGarcía Ruano, José L. 
Admission datedc.date.accessioned2018-12-20T14:13:53Z
Available datedc.date.available2018-12-20T14:13:53Z
Publication datedc.date.issued2013
Cita de ítemdc.identifier.citationTetrahedron Asymmetry, Volumen 24, Issue 1, 2018, Pages 56-61
Identifierdc.identifier.issn09574166
Identifierdc.identifier.issn1362511X
Identifierdc.identifier.other10.1016/j.tetasy.2012.11.017
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/155003
Abstractdc.description.abstractDiels-Alder cycloaddition of 8,8-dimethylnaphthalene-1,4,5(8H)-trione with diastereomeric hydroxysulfinyldienes proceeded with high yields and good π-facial and regioselectivities. The hydroxysulfoxide moiety controls the regio- and stereoselectivities, through hydrogen bonds in the suggested transition state. © 2012 Elsevier Ltd. All rights reserved.
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 Asymmetry
Keywordsdc.subjectCatalysis
Keywordsdc.subjectPhysical and Theoretical Chemistry
Keywordsdc.subjectOrganic Chemistry
Keywordsdc.subjectInorganic Chemistry
Títulodc.titleRemote regio- and stereocontrol by the sulfinyl group: Diels-Alder reaction of sulfinyl dienols and 8,8-dimethylnaphthalene-1,4,5(8H)-trione
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