Remote regio- and stereocontrol by the sulfinyl group: Diels–Alder reaction of sulfinyl dienols and 8,8-dimethylnaphthalene-1,4,5(8H)-trione

dc.creatorAlmodovar, Iriux
dc.creatorCardona, Wilson
dc.creatorDelgado Castro, Tomás
dc.creatorZapata Torres, Gerald Amilcar
dc.creatorCaroli Rezende, Marcos
dc.creatorAraya Maturana, Ramiro
dc.creatorMaestro, M. Carmen
dc.creatorGarcía Ruano, José L.
dc.date.accessioned2014-03-12T20:36:14Z
dc.date.available2014-03-12T20:36:14Z
dc.date.created2014-03-12T20:36:14Z
dc.date.issued2013
dc.identifierTetrahedron: Asymmetry 24 (2013) 56–61
dc.identifierdoi10.1016/j.tetasy.2012.11.017
dc.identifierhttps://repositorio.uchile.cl/handle/2250/121855
dc.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.
dc.languageen
dc.publisherElsevier
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.titleRemote regio- and stereocontrol by the sulfinyl group: Diels–Alder reaction of sulfinyl dienols and 8,8-dimethylnaphthalene-1,4,5(8H)-trione
dc.typeArtículo de revista


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