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Cycloaddition reactions of nitrosoalkenes, azoalkenes and nitrile oxides mediated by hydrotalcite

dc.contributor.authorLemos, A.
dc.contributor.authorLourenço, J. P.
dc.date.accessioned2012-03-13T23:23:41Z
dc.date.available2012-03-13T23:23:41Z
dc.date.issued2010
dc.date.updated2012-03-12T17:45:40Z
dc.description.abstractMg:Al 3:1 hydrotalcite (Ht), used in catalytic quantities, promotes the generation of nitrosoalkenes, azoalkenes and nitrile oxides. These can be intercepted in situ by heterocycles and olefins in [4+2] and [3+2] cycloaddition reactions, producing dihydro-1,2-oxazines, tetrahydropyridazines and isoxazolines. The regeneration and reuse of Ht without loss of activity and the absence of organic solvent are the main advantages of this methodology.por
dc.identifier.citationARKIVOC, v, 170-182, 2010.por
dc.identifier.otherAUT: ALE01411; JLO01215;
dc.identifier.urihttp://hdl.handle.net/10400.1/939
dc.language.isoengpor
dc.peerreviewedyespor
dc.subjectCycloadditionpor
dc.subjectHydrotalcitepor
dc.titleCycloaddition reactions of nitrosoalkenes, azoalkenes and nitrile oxides mediated by hydrotalcitepor
dc.typejournal article
dspace.entity.typePublication
person.familyNameLemos
person.familyNameLourenço
person.givenNameAmerico
person.givenNameJoão P.
person.identifier634248
person.identifier.ciencia-idA81D-6DC7-31E4
person.identifier.ciencia-idF81F-A1F0-2A7C
person.identifier.orcid0000-0001-9588-4555
person.identifier.orcid0000-0002-0501-6672
person.identifier.ridB-4892-2008
person.identifier.ridA-7758-2008
person.identifier.scopus-author-id11139694000
person.identifier.scopus-author-id57195730600
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublication70dfe028-027a-4dec-b6e3-1a49c9be9e60
relation.isAuthorOfPublicationf66ab886-d989-4c1d-9550-527507723c26
relation.isAuthorOfPublication.latestForDiscoveryf66ab886-d989-4c1d-9550-527507723c26

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