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Efficient synthesis of spiroisoxazoline oxindoles

dc.contributor.authorRibeiro, Carlos J. A.
dc.contributor.authorKumar, S. Praveen
dc.contributor.authorMoreira, Rui
dc.contributor.authorSantos, Maria M. M.
dc.date.accessioned2013-04-02T13:51:01Z
dc.date.available2013-04-02T13:51:01Z
dc.date.issued2012
dc.descriptionAcknowledgments: We thank Fundação para a Ciência e Tecnologia (Portugal) for financial support [Projects PTDC/QUI-QUI/111664/2009 and PTDC/SAU-FAR/110848/2009 and Fellowships SFRH/BD/69258/2010 and SFRH/BPD/44481/2008].por
dc.description.abstractThe synthesis of spiroisoxazoline oxindoles containing ester groups at position 4′ and aromatic or ester groups at position 3′ of the isoxazoline ring is reported. The compounds were synthesized in yields up to 94% by 1,3-dipolar cycloaddition of 3-methylene indolin-2-ones and chlorooximes in the presence of triethylamine or zinc.por
dc.description.sponsorshipFundação para a Ciência e Tecnologia (Portugal)por
dc.identifier.citationTetrahedron Letters 53 (2012) 281–284por
dc.identifier.issn0040-4039
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2011.10.139
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0040403911018934
dc.language.isoengpor
dc.peerreviewedyespor
dc.relationEnantioselective synthesis of indole alkaloids and their application as NMDA antagonists
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.tetlet.2011.10.139por
dc.subjectSpirooxindolepor
dc.subjectIsoxazolinepor
dc.subject1,3-Dipolar cycloadditionpor
dc.subjectChlorooximepor
dc.subjectZincpor
dc.titleEfficient synthesis of spiroisoxazoline oxindolespor
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleEnantioselective synthesis of indole alkaloids and their application as NMDA antagonists
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FQUI-QUI%2F111664%2F2009/PT
oaire.citation.endPage284por
oaire.citation.startPage281por
oaire.citation.titleTetrahedron Letterspor
oaire.citation.volume53por
oaire.fundingStream3599-PPCDT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor
relation.isProjectOfPublication07316c55-1daa-4b66-aa2f-3077d53d7cda
relation.isProjectOfPublication.latestForDiscovery07316c55-1daa-4b66-aa2f-3077d53d7cda

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