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Reactions of azoalkenes derived from hydrazones of ethyl bromopyruvate with electron rich alkenes and heterocycles

dc.contributor.authorClarke, S
dc.contributor.authorGilchrist, Thomas L.
dc.contributor.authorLemos, A.
dc.contributor.authorRoberts, Tony G.
dc.date.accessioned2012-03-09T15:20:24Z
dc.date.available2012-03-09T15:20:24Z
dc.date.issued1991
dc.date.updated2012-02-27T17:41:06Z
dc.description.abstractThree hydrazones of ethyl bromopyruvate, the dinitrophenylhydrazone 2a, the toluene-4-sulphonylhydrazone 2b and the t-butoxycarbonylhydrazone 2c, have been reacted with a series of nucleophilic alkenes and heterocycles in the presence of sodium carbonate. Azoalkenes 3 are presumed as intermediates and adducts have been isolated. The azoalkenes derived from hydrazones 2a and 2c are found to be useful electrophiles and electrophilic dienes.
dc.identifier.citationClarke, S. Reactions of azoalkenes derived from hydrazones of ethyl bromopyruvate with electron rich alkenes and heterocycles, Tetrahedron, 47, 29, 5615-5624, 1991.por
dc.identifier.issn00404020
dc.identifier.otherAUT: ALE01411;
dc.identifier.urihttp://hdl.handle.net/10400.1/934
dc.language.isoengpor
dc.peerreviewedyespor
dc.subjectCicloadiçãopor
dc.subjectDiels-Alderpor
dc.subjectHeterocyclespor
dc.titleReactions of azoalkenes derived from hydrazones of ethyl bromopyruvate with electron rich alkenes and heterocyclespor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage5624
oaire.citation.issue29
oaire.citation.startPage5615
oaire.citation.titleTetrahedron
oaire.citation.volume47
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
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublication70dfe028-027a-4dec-b6e3-1a49c9be9e60
relation.isAuthorOfPublication.latestForDiscovery70dfe028-027a-4dec-b6e3-1a49c9be9e60

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