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Diels–Alder reactions of 3-(1H-tetrazol-5-yl)-nitrosoalkenes: synthesis of functionalized 5-(substituted)-1H-tetrazoles

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dc.contributor.authorLopes, Susana M. M.
dc.contributor.authorPalacios, Francisco
dc.contributor.authorLemos, A.
dc.contributor.authorMelo, Teresa M. V. D. Pinho e
dc.date.accessioned2012-04-18T15:34:16Z
dc.date.available2012-04-18T15:34:16Z
dc.date.issued2011
dc.date.updated2012-04-13T12:45:49Z
dc.description.abstractA general route to 1,2-oxazines and open chain oximes bearing a 1H-tetrazolyl substituent via DielseAlder reaction of 3-(tetrazol-5-yl)-nitrosoalkenes is reported. It was also demonstrated that reduction of these adducts followed by deprotection of the tetrazolyl group give 5-(1-aminoalkyl)-1H-tetrazoles, a-amino acid analogues.por
dc.identifier.citationLopes, Susana M.M.; Palacios, Francisco; Lemos, A.; Melo, Teresa M.V.D.Pinho e. Diels–Alder reactions of 3-(1H-tetrazol-5-yl)-nitrosoalkenes: synthesis of functionalized 5-(substituted)-1H-tetrazoles. Tetrahedron, 67, 46, 8902-8909, 2011.por
dc.identifier.issn00404020
dc.identifier.otherAUT: ALE01411;
dc.identifier.urihttp://hdl.handle.net/10400.1/1046
dc.language.isoengpor
dc.peerreviewedyespor
dc.subjectCicloadiçãopor
dc.subjectDiels-Alderpor
dc.subjectHeterocyclespor
dc.titleDiels–Alder reactions of 3-(1H-tetrazol-5-yl)-nitrosoalkenes: synthesis of functionalized 5-(substituted)-1H-tetrazolespor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage8909por
oaire.citation.issue67(46)por
oaire.citation.startPage8902por
oaire.citation.titleTetrahedronpor
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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