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Intramolecularity of the thermal rearrangement of allyloxytetrazoles to N-allyltetrazolones†

1997Journal article Restricted access
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dc.contributor.authorCristiano, Maria Lurdes Santos
dc.contributor.authorJohnstone, Robert A. W.
dc.date.accessioned2014-06-11T13:09:40Z
dc.date.available2014-06-11T13:09:40Z
dc.date.issued1997
dc.date.updated2014-06-05T09:24:49Z
dc.description.abstractThe intramolecularity of the thermal rearrangement of 1-aryl-5-allyloxy-1H-tetrazoles 1 to 1-aryl-4-allyl-1,4-dihydrotetrazol-5-ones 2 has been investigated through cross-over studies: the results support the hypothesis for a concerted sigmatropic rearrangement occurring through a highly polar transition state, in which a partially positively charged allyl group migrates from oxygen to nitrogen, without leaving the solvent cage.por
dc.identifier.citationCristiano, M. Lurdes S.; Johnstone, Robert A. W. Intramolecularity of the Thermal Rearrangement of Allyloxytetrazoles to N-Allyltetrazolones†, Journal of Chemical Research, 5, 164-165, 1997.por
dc.identifier.doihttp://dx.doi.org/10.1039/A608333A
dc.identifier.otherAUT: MCR00716;
dc.identifier.urihttp://hdl.handle.net/10400.1/4267
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherRoyal Society of Chemistrypor
dc.relation.publisherversionView Article Onlinepor
dc.titleIntramolecularity of the thermal rearrangement of allyloxytetrazoles to N-allyltetrazolones†por
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage165por
oaire.citation.startPage164por
oaire.citation.titleJournal of Chemical Researchpor
oaire.citation.volume5por
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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