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dc.contributor.CRUESPUNIVERSIDADE ESTADUAL DE CAMPINASpt_BR
dc.contributor.authorunicampRodrigues Junior, Manoel Trindade-
dc.contributor.authorunicampSantos, Marilia Simão dos-
dc.contributor.authorunicampSantos, Hugo dos-
dc.contributor.authorunicampCoelho, Fernando Antonio Santos-
dc.typeArtigopt_BR
dc.title1,1 '-Carbonyldiimidazole mediates the synthesis of N-substituted imidazole derivatives from Morita-Baylis-Hillman adductspt_BR
dc.contributor.authorRodrigues, M. T.-
dc.contributor.authorSantos, H.-
dc.contributor.authorCoelho, F.-
dc.contributor.authorSantos, M. S.-
dc.subjectLíquidos iônicospt_BR
dc.subjectImidazolpt_BR
dc.subjectMorita-Baylis-Hillmanpt_BR
dc.subjectReação diastereosseletivapt_BR
dc.subject.otherlanguageIonic liquidspt_BR
dc.subject.otherlanguageImidazolept_BR
dc.subject.otherlanguageMorita-Baylis-Hillmanpt_BR
dc.subject.otherlanguageDiastereoselective reactionpt_BR
dc.description.abstractIn this Letter, we describe a simple and straightforward method for the synthesis of N-substituted imidazole derivatives. 1,1-carbonyldiimidazole mediates the process, which requires no activation group step. We obtained imidazole derivatives in high yields and with short reaction times. To demonstrate the synthetic significance of the aforementioned compounds, we also describe the synthesis of novel ionic liquids from these derivativespt_BR
dc.relation.ispartofTetrahedron letters: the international journal for the rapid publication of all preliminary communications in organic chemistrypt_BR
dc.relation.ispartofabbreviationTetrahedron lett.pt_BR
dc.publisher.cityOxfordpt_BR
dc.publisher.countryReino Unidopt_BR
dc.publisherElsevierpt_BR
dc.date.issued2014-
dc.date.monthofcirculationJan.pt_BR
dc.language.isoengpt_BR
dc.description.volume55pt_BR
dc.description.issuenumber1pt_BR
dc.description.firstpage180pt_BR
dc.description.lastpage183pt_BR
dc.rightsAbertopt_BR
dc.sourceWOSpt_BR
dc.identifier.issn0040-4039pt_BR
dc.identifier.eissn1873-3581pt_BR
dc.identifier.doi10.1016/j.tetlet.2013.10.146pt_BR
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S004040391301914Xpt_BR
dc.description.sponsorshipCONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQpt_BR
dc.description.sponsorshipFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESPpt_BR
dc.date.available2020-11-11T14:31:41Z-
dc.date.accessioned2020-11-11T14:31:41Z-
dc.description.provenanceSubmitted by Cintia Oliveira de Moura (cintiaom@unicamp.br) on 2020-11-11T14:31:41Z No. of bitstreams: 0. Added 1 bitstream(s) on 2021-02-16T16:52:54Z : No. of bitstreams: 1 000329960500038.pdf: 930027 bytes, checksum: 1185c437786a40db99c3c28e7ea866dd (MD5)en
dc.description.provenanceMade available in DSpace on 2020-11-11T14:31:41Z (GMT). No. of bitstreams: 0 Previous issue date: 2014en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/352163-
dc.contributor.departmentsem informaçãopt_BR
dc.contributor.departmentsem informaçãopt_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.contributor.unidadeInstituto de Químicapt_BR
dc.identifier.source000329960500038pt_BR
dc.creator.orcidsem informaçãopt_BR
dc.creator.orcid0000-0002-0269-4902pt_BR
dc.creator.orcid0000-0002-7411-5180pt_BR
dc.creator.orcid0000-0003-1800-1549pt_BR
dc.type.formArtigopt_BR
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