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Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/352998
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dc.contributor.CRUESPUNIVERSIDADE ESTADUAL DE CAMPINASpt_BR
dc.contributor.authorunicampDias, Luiz Carlos-
dc.contributor.authorunicampKuroishi, Paula Kishi-
dc.contributor.authorunicampLucca Júnior, Emilio Carlos de-
dc.typeArtigopt_BR
dc.titleThe total synthesis of (-)-cryptocaryol Apt_BR
dc.contributor.authorDias, L. C.-
dc.contributor.authorKuroishi, P. K.-
dc.contributor.authorde Lucca Junior, E. C.-
dc.subjectCriptocariol Apt_BR
dc.subjectReação aldólicapt_BR
dc.subject.otherlanguageCryptocaryol Apt_BR
dc.subject.otherlanguageAldol reactionpt_BR
dc.description.abstractA stereoselective total synthesis of (-)-cryptocaryol A (1) is described. Key features of the 17-step route include the use of three boron-mediated aldol reaction-reduction sequences to control all stereocenters and an Ando modification of the Horner-Wadsworth-Emmons olefination that permitted the installation of the Z double bond of the alpha-pyrone ringpt_BR
dc.relation.ispartofOrganic & biomolecular chemistrypt_BR
dc.publisher.cityCambridge, MApt_BR
dc.publisher.countryEstados Unidospt_BR
dc.publisherRoyal Society of Chemistrypt_BR
dc.date.issued2015-
dc.date.monthofcirculationFeb.pt_BR
dc.language.isoengpt_BR
dc.description.volume13pt_BR
dc.description.issuenumber12pt_BR
dc.description.firstpage3575pt_BR
dc.description.lastpage3584pt_BR
dc.rightsAbertopt_BR
dc.sourceWOSpt_BR
dc.identifier.issn1477-0520pt_BR
dc.identifier.eissn1477-0539pt_BR
dc.identifier.doi10.1039/c5ob00080gpt_BR
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2015/OB/C5OB00080Gpt_BR
dc.description.sponsorshipCONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQpt_BR
dc.description.sponsorshipCOORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPESpt_BR
dc.description.sponsorshipFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESPpt_BR
dc.description.sponsordocumentnumber573.564/2008-6pt_BR
dc.description.sponsordocumentnumbersem informaçãopt_BR
dc.description.sponsordocumentnumber2012/02230-0; 2013/07600-3pt_BR
dc.date.available2020-12-04T18:55:18Z-
dc.date.accessioned2020-12-04T18:55:18Z-
dc.description.provenanceSubmitted by Cintia Oliveira de Moura (cintiaom@unicamp.br) on 2020-12-04T18:55:18Z No. of bitstreams: 0. Added 1 bitstream(s) on 2021-02-19T19:00:08Z : No. of bitstreams: 1 000351352100008.pdf: 1309335 bytes, checksum: 01d3352469d3f8729c1b531a849b3c42 (MD5)en
dc.description.provenanceMade available in DSpace on 2020-12-04T18:55:18Z (GMT). No. of bitstreams: 0 Previous issue date: 2015en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/352998-
dc.contributor.departmentDepartamento de Química Orgânicapt_BR
dc.contributor.departmentsem informaçãopt_BR
dc.contributor.departmentDepartamento de Química Orgânicapt_BR
dc.contributor.unidadeInstituto de Químicapt_BR
dc.contributor.unidadeInstituto de Químicapt_BR
dc.contributor.unidadeInstituto de Químicapt_BR
dc.subject.keywordOxygenated Methyl Ketonespt_BR
dc.subject.keywordDirected Reductionpt_BR
dc.identifier.source000351352100008pt_BR
dc.creator.orcid0000-0003-0628-9928pt_BR
dc.creator.orcid0000-0001-7082-6586pt_BR
dc.creator.orcid0000-0002-7732-3559pt_BR
dc.type.formArtigopt_BR
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