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Reactions of Azovinylphosphonates with Nucleophilic Alkenes and Heterocycles: synthesis of Tetrahydropyridazine-3-phosphonate and 2-Substituted-1-hydrazonoethylphosphonate derivatives

dc.contributor.authorLemos, A.
dc.contributor.authorLopes, Marta
dc.date.accessioned2012-04-18T15:38:36Z
dc.date.available2012-04-18T15:38:36Z
dc.date.issued2008
dc.date.updated2012-04-13T12:30:17Z
dc.description.abstractTransient azovinylphosphonates, generated in situ by base induced dehydrohalogenation of the corresponding 2-bromo- and 2-chloro-acetylphosphonate- tertbutoxycarbonyl hydrazones are intercepted by electron rich alkenes and heterocycles in hetero Diels-Alder reactions, producing tetrahydopyridazine-3-phosphonates or open chain α-hydrazono phosphonates.por
dc.identifier.citationLemos, A.; Lopes, Marta. Reactions of Azovinylphosphonates with Nucleophilic Alkenes and Heterocycles: synthesis of Tetrahydropyridazine-3-phosphonate and 2-Substituted-1-hydrazonoethylphosphonate derivatives. Phosphorus, Sulfur Silicon Relat. Elem. 183, 11, 2882-2890, 2008.por
dc.identifier.otherAUT: ALE01411;
dc.identifier.urihttp://hdl.handle.net/10400.1/1048
dc.language.isoengpor
dc.peerreviewedyespor
dc.subjectAzoalkenepor
dc.subjectCicloadiçãopor
dc.subjectHydrazonophosphonatepor
dc.subjectAminofosfonatospor
dc.subjectHeterocyclespor
dc.subjectPiridazina fosfonatopor
dc.titleReactions of Azovinylphosphonates with Nucleophilic Alkenes and Heterocycles: synthesis of Tetrahydropyridazine-3-phosphonate and 2-Substituted-1-hydrazonoethylphosphonate derivativespor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage2890por
oaire.citation.issue183(11)por
oaire.citation.startPage2882por
oaire.citation.titlePhosphorus, Sulfur, and Silicon and the Related Elementspor
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.rightsrestrictedAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublication70dfe028-027a-4dec-b6e3-1a49c9be9e60
relation.isAuthorOfPublication.latestForDiscovery70dfe028-027a-4dec-b6e3-1a49c9be9e60

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