dc.creatorAugusto, J
dc.creatorRodrigues, R
dc.creatorMoran, PJS
dc.creatorMilagre, CDF
dc.creatorUrsini, CV
dc.date2004
dc.dateAPR 26
dc.date2014-11-15T09:40:32Z
dc.date2015-11-26T17:19:12Z
dc.date2014-11-15T09:40:32Z
dc.date2015-11-26T17:19:12Z
dc.date.accessioned2018-03-29T00:06:52Z
dc.date.available2018-03-29T00:06:52Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 45, n. 18, n. 3579, n. 3582, 2004.
dc.identifier0040-4039
dc.identifierWOS:000221022500009
dc.identifier10.1016/j.tetlet.2004.03.062
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/61688
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/61688
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/61688
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1282846
dc.descriptionA synthetic study was carried out to obtain epimers of a protected 2,4-dihydroxy-3-methylpentanoic ester 9, which is a central building block of the immunomodulator (+)-conagenin 1. The configuration of the three contiguous stereogenic centers was determined by NMR measurements and comparison with the stereogenic centers of lactone 10. (C) 2004 Elsevier Ltd. All rights reserved.
dc.description45
dc.description18
dc.description3579
dc.description3582
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.subjectconagenin
dc.subjectPHB-biopolymer
dc.subjectbeta-methylene-alpha-keto ester
dc.subjecthydrogenation
dc.subjectMolecular-weight Immunomodulator
dc.subjectStereoselective Synthesis
dc.subjectStreptomyces-roseosporus
dc.subjectAcyclic Stereoselection
dc.subject(+)-conagenin
dc.subjectEsters
dc.subjectAcids
dc.subjectAldehydes
dc.subjectAlcohols
dc.titleDiastereo- and enantioselective synthesis of a conagenin skeletal amide moiety
dc.typeArtículos de revistas


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