dc.creatorDias, LC
dc.creatorMeira, PRR
dc.date2000
dc.dateJAN
dc.date2014-12-02T16:29:04Z
dc.date2015-11-26T16:38:35Z
dc.date2014-12-02T16:29:04Z
dc.date2015-11-26T16:38:35Z
dc.date.accessioned2018-03-28T23:21:58Z
dc.date.available2018-03-28T23:21:58Z
dc.identifierSynlett. Georg Thieme Verlag, n. 1, n. 37, n. 40, 2000.
dc.identifier0936-5214
dc.identifierWOS:000086556300007
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/63102
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/63102
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/63102
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1272287
dc.descriptionAddition of chiral allylsilane 4 to chiral N-Boc-alpha-amino aldehydes in the presence of SnCl4 in CH2Cl2 at -78 degrees C affords 1,2-syn homoallylic alcohols, potential intermediates for the synthesis of hydroxyethylene peptide isosteres. The diastereoselectivity depends on the aldehyde absolute configuration, with (R)-alpha-aminoaldehydes (matched case/anti-Felkin addition) exhibiting higher stereoselectivity than its enantiomer (mismatched case/Felkin addition).
dc.descriptiono TEXTO COMPLETO DESTE ARTIGO, ESTARÁ DISPONÍVEL À PARTIR DE AGOSTO DE 2015.
dc.description1
dc.description37
dc.description40
dc.languageen
dc.publisherGeorg Thieme Verlag
dc.publisherStuttgart
dc.publisherAlemanha
dc.relationSynlett
dc.relationSynlett
dc.rightsembargo
dc.sourceWeb of Science
dc.subjectchiral allylsilane
dc.subjectalpha-amino aldehydes
dc.subjectdipeptide isosteres
dc.subjecthomoallylic alcohols
dc.subjectoxazolidines
dc.subjectHydroxyethylene Dipeptide Isosteres
dc.subjectHiv-1 Protease Inhibitors
dc.subjectSubstituted Aldehydes
dc.subjectAsymmetric-synthesis
dc.subjectOrganic-synthesis
dc.subjectAcid
dc.subjectAminoaldehydes
dc.subjectConvenient
dc.subjectVersatile
dc.titleChiral allylsilane additions to chiral N-Boc-alpha-amino aldehydes
dc.typeArtículos de revistas


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