dc.creatorDias, LC
dc.creatorFattori, J
dc.creatorPerez, CC
dc.date2008
dc.date41640
dc.date2014-11-15T12:58:55Z
dc.date2015-11-26T16:11:20Z
dc.date2014-11-15T12:58:55Z
dc.date2015-11-26T16:11:20Z
dc.date.accessioned2018-03-28T22:59:50Z
dc.date.available2018-03-28T22:59:50Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 49, n. 3, n. 557, n. 561, 2008.
dc.identifier0040-4039
dc.identifierWOS:000253061900035
dc.identifier10.1016/j.tetlet.2007.11.072
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/76704
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/76704
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/76704
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1267064
dc.descriptionWe wish to describe here the diastereoselective reaction between chiral N-Boc-alpha-amino aldehydes and achiral allyltrichlorostannanes leading to 1,2-syn-N-Boc-alpha-amino alcohols, which are treated with catalytic amounts of OSO4 in the presence of NaIO4 to provide the corresponding 4-N-Boc-amino-3-hydroxy ketones. (C) 2007 Elsevier Ltd. All rights reserved.
dc.description49
dc.description3
dc.description557
dc.description561
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.subjectallyltrichlorostannane
dc.subjectallylsilanes
dc.subjectaminoketones
dc.subjectoxazolidinones
dc.subjectAlpha-amino Aldehydes
dc.subjectHydroxyethylene Dipeptide Isosteres
dc.subjectAsymmetric Induction
dc.subjectChiral Aldehydes
dc.subjectDerivatives
dc.subjectEsters
dc.subjectAcids
dc.subjectSphingosine
dc.subjectInhibition
dc.subjectReduction
dc.titleAddition of allyltrichlorostannanes to aldehydes: application in the synthesis of 4-N-Boc-amino-3-hydroxy ketones
dc.typeArtículos de revistas


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