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Ethyl 7-Acetyl-8a-methyl-3-(1-phenyl-1H-tetrazol-5-yl)-1,4,4a,5,6,8a-hexahydro-7H-pyrano[2,3-c]pyridazine-1-carboxylate

dc.contributor.authorLopes, Susana M. M.
dc.contributor.authorLemos, Americo
dc.contributor.authorPaixão, José A.
dc.contributor.authorPinho e Melo, Teresa M. V. D.
dc.date.accessioned2022-03-28T11:20:23Z
dc.date.available2022-03-28T11:20:23Z
dc.date.issued2022-02-10
dc.date.updated2022-03-24T14:46:47Z
dc.description.abstractThe Diels–Alder reaction of ethyl 3-(1-phenyl-1<i>H</i>-tetrazol-5-yl-1,2-diaza-1,3-butadiene-1-carboxylate with 2-acetyl-6-methyl-2,3-dihydro-4<i>H</i>-pyran (methyl vinyl ketone dimer) regioselectively afforded the corresponding 3-(tetrazol-5-yl)-hexahydro-7<i>H</i>-pyrano[2,3-<i>c</i>]pyridazine in quantitative yield. An X-ray crystal structure of this cycloadduct is reported.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationMolbank 2022 (1): M1338 (2022)pt_PT
dc.identifier.doi10.3390/M1338pt_PT
dc.identifier.issn1422-8599
dc.identifier.urihttp://hdl.handle.net/10400.1/17725
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationCoimbra Chemistry Center
dc.relationCoimbra Chemistry Center
dc.relationCenter for Physics of the University of Coimbra
dc.relationCenter for Physics of the University of Coimbra
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectTetrazolespt_PT
dc.subjectDiaza-1,3-butadienept_PT
dc.subjectPyrano[2,3-c]pyridazinept_PT
dc.subjectMethyl vinyl ketone dimerpt_PT
dc.subjectDiels-alder reactionspt_PT
dc.subjectX-ray structurept_PT
dc.titleEthyl 7-Acetyl-8a-methyl-3-(1-phenyl-1H-tetrazol-5-yl)-1,4,4a,5,6,8a-hexahydro-7H-pyrano[2,3-c]pyridazine-1-carboxylatept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleCoimbra Chemistry Center
oaire.awardTitleCoimbra Chemistry Center
oaire.awardTitleCenter for Physics of the University of Coimbra
oaire.awardTitleCenter for Physics of the University of Coimbra
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F00313%2F2020/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F00313%2F2020/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04564%2F2020/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04564%2F2020/PT
oaire.citation.issue1pt_PT
oaire.citation.startPageM1338pt_PT
oaire.citation.titleMolbankpt_PT
oaire.citation.volume2022pt_PT
oaire.fundingStream6817 - DCRRNI ID
oaire.fundingStream6817 - DCRRNI ID
oaire.fundingStream6817 - DCRRNI ID
oaire.fundingStream6817 - DCRRNI ID
person.familyNameLemos
person.givenNameAmerico
person.identifier.ciencia-idA81D-6DC7-31E4
person.identifier.orcid0000-0001-9588-4555
person.identifier.ridB-4892-2008
person.identifier.scopus-author-id11139694000
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
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relation.isAuthorOfPublication.latestForDiscovery70dfe028-027a-4dec-b6e3-1a49c9be9e60
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