Stereoselective synthesis of the 6,6-spiroketal core of CP-61,405 (routiennocin)

dc.creatorDias, LC
dc.creatorCorreia, VG
dc.creatorFinelli, FG
dc.date2007
dc.dateOCT 22
dc.date2014-11-18T21:46:59Z
dc.date2015-11-26T17:54:39Z
dc.date2014-11-18T21:46:59Z
dc.date2015-11-26T17:54:39Z
dc.date.accessioned2018-03-29T00:38:21Z
dc.date.available2018-03-29T00:38:21Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 48, n. 43, n. 7683, n. 7686, 2007.
dc.identifier0040-4039
dc.identifierWOS:000250310800029
dc.identifier10.1016/j.tetlet.2007.08.087
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/75222
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/75222
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/75222
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1290825
dc.descriptionA convergent and efficient synthesis of the 6,6-spiroketal core of the ionophore antibiotic CP-61,405 (routiennocin) is described. The synthesis required 10 steps from N-propionyl oxazolidinone (S)-8 and produced the desired spiroketal in 36% overall yield. (C) 2007 Elsevier Ltd. All rights reserved.
dc.description48
dc.description43
dc.description7683
dc.description7686
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.subjectspiroketal
dc.subjectionophore antibiotic
dc.subjectaldol reaction
dc.subjectEnantioselective Aldol Condensations
dc.subjectSpirofungin-a
dc.subjectIonophore
dc.subjectSpiroacetals
dc.subjectSpiroketals
dc.subjectChemistry
dc.subjectComplex
dc.subjectAmides
dc.titleStereoselective synthesis of the 6,6-spiroketal core of CP-61,405 (routiennocin)
dc.typeArtículos de revistas


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