Allyltrichlorostannane additions to chiral dipeptide aldehydes

dc.creatorDias, LC
dc.creatorFerreira, E
dc.date2001
dc.dateOCT 8
dc.date2014-11-14T22:25:02Z
dc.date2015-11-26T16:08:41Z
dc.date2014-11-14T22:25:02Z
dc.date2015-11-26T16:08:41Z
dc.date.accessioned2018-03-28T22:57:15Z
dc.date.available2018-03-28T22:57:15Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 42, n. 41, n. 7159, n. 7162, 2001.
dc.identifier0040-4039
dc.identifierWOS:000171278200008
dc.identifier10.1016/S0040-4039(01)01502-7
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/77160
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/77160
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/77160
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1266423
dc.descriptionThe first examples of successful allylsilane additions to chiral dipeptide aldehydes are described. Treatment of allylsilanes with tin tetrachloride at room temperature affords allyltrichlorostarnnane intermediates that reacts with dipeptide aldehydes to give 1,2-syn-homoallylic alcohols, potential intermediates for the synthesis of hydroxyethylene dipeptide isosteres. (C) 2001 Elsevier Science Ltd. All rights reserved.
dc.description42
dc.description41
dc.description7159
dc.description7162
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.subjectAlpha-amino Aldehydes
dc.subjectHiv-protease Inhibitors
dc.subjectAllylsilane Additions
dc.subjectSubstituted Aldehydes
dc.subjectAminoaldehydes
dc.subjectVersatile
dc.subjectIsosteres
dc.subjectCore
dc.titleAllyltrichlorostannane additions to chiral dipeptide aldehydes
dc.typeArtículos de revistas


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