dc.creatorCoelho, F
dc.creatorRossi, RC
dc.date2002
dc.dateAPR 8
dc.date2014-11-20T01:48:54Z
dc.date2015-11-26T17:11:47Z
dc.date2014-11-20T01:48:54Z
dc.date2015-11-26T17:11:47Z
dc.date.accessioned2018-03-29T00:00:16Z
dc.date.available2018-03-29T00:00:16Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 43, n. 15, n. 2797, n. 2800, 2002.
dc.identifier0040-4039
dc.identifierWOS:000175108000031
dc.identifier10.1016/S0040-4039(02)00351-9
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/54329
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/54329
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/54329
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1281181
dc.descriptionIn this communication we describe a straightforward and diastereoselective approach to prepare functionalised oxazolidin-2-ones from Baylis-Hillinan adducts. A stereoselective synthesis of a highly Substituted vicinal aminoalcohol and a formal synthesis of a chloramphenicol derivative are also described. (C) 2002 Elsevier Science Ltd. All rights reserved.
dc.description43
dc.description15
dc.description2797
dc.description2800
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron Letters
dc.relationTetrahedron Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectoxazolidin-2-one
dc.subjectBaylis-Hillman reaction
dc.subjectchloramphenicol derivative
dc.subjectChiral Auxiliary
dc.subjectEnantioselective Syntheses
dc.subjectAsymmetric-synthesis
dc.subjectCarboxylic-acids
dc.subjectOxazolidinones
dc.subjectOxidation
dc.subjectAldehydes
dc.subject2-oxazolidinone
dc.subjectRearrangement
dc.subjectCycloaddition
dc.titleAn approach to oxazolidin-2-ones from the Baylis-Hillman adducts. Formal synthesis of a chloramphenicol derivative
dc.typeArtículos de revistas


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