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A kinetic investigation of the thermal rearrangement of allyloxytetrazoles to N-allyltetrazolones

dc.contributor.authorCristiano, Maria Lurdes Santos
dc.contributor.authorJohnstone, Robert A. W.
dc.date.accessioned2014-06-09T13:20:02Z
dc.date.available2014-06-09T13:20:02Z
dc.date.issued1997
dc.date.updated2014-06-05T09:17:55Z
dc.description.abstractThe mechanism of the thermal rearrangement of 1-aryl-5-allyloxytetrazoles 1 to give 1-aryl-4-allyltetrazolones 2 in very high yield has been investigated through kinetic studies in one polar and one less polar solvent. The results suggest mainly a concerted [3,3] sigmatropic process, in which a partially positively charged allyl group migrates from oxygen to nitrogen, similar to the polar transition state found in the Claisen rearrangement.por
dc.identifier.citationCristiano, M. Lurdes S.; Johnstone, Robert A. W. A kinetic investigation of the thermal rearrangement of allyloxytetrazoles to N-allyltetrazolones, Journal of the Chemical Society, Perkin Transactions 2, 3, 489-494, 1997.por
dc.identifier.issn0300-9580
dc.identifier.otherAUT: MCR00716;
dc.identifier.urihttp://hdl.handle.net/10400.1/4256
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherChemical Societypor
dc.relation.publisherversionView Article Onlinepor
dc.titleA kinetic investigation of the thermal rearrangement of allyloxytetrazoles to N-allyltetrazolonespor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage494por
oaire.citation.issue3por
oaire.citation.startPage489por
oaire.citation.titlePerkin Transactions 2por
oaire.citation.volume2por
person.familyNameCristiano
person.givenNameMaria de Lurdes
person.identifier.ciencia-idE411-6006-5A01
person.identifier.orcid0000-0002-9447-2855
person.identifier.ridG-2345-2012
person.identifier.scopus-author-id9238724800
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicationb16751a6-748e-44b0-9c59-058cbd5b2cc3
relation.isAuthorOfPublication.latestForDiscoveryb16751a6-748e-44b0-9c59-058cbd5b2cc3

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