Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/5241
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dc.contributor.authorPinho e Melo, Teresa M. V. D.-
dc.contributor.authorLopes, Cláudia S. J.-
dc.contributor.authorGonsalves, António M. d'A. Rocha-
dc.date.accessioned2008-09-01T15:06:22Z-
dc.date.available2008-09-01T15:06:22Z-
dc.date.issued2000en_US
dc.identifier.citationTetrahedron Letters. 41:37 (2000) 7217-7220en_US
dc.identifier.urihttps://hdl.handle.net/10316/5241-
dc.description.abstractNucleophilic substitution reactions of 2-halo-2H-azirine with potassium phthalimide and aniline allowed the preparation of new substituted 2H-azirines. The reactions of 2-bromo-3-phenyl-2H-azirine-2-carboxylate with methylamine led to the synthesis of [alpha]-diimines and from the reaction with water, a 3-oxazoline was obtained.en_US
dc.description.urihttp://www.sciencedirect.com/science/article/B6THS-4152YMR-K/1/e94005b66b66b6820ad27458f2562edden_US
dc.format.mimetypeaplication/PDFen
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subject2H-azirinesen_US
dc.subject[alpha]-diiminesen_US
dc.subject3-oxazolineen_US
dc.titleSynthesis and reactivity of 2-halo-2H-azirines towards nucleophilesen_US
dc.typearticleen_US
dc.identifier.doi10.1002/chin.200048131-
uc.controloAutoridadeSim-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-3256-4954-
crisitem.author.orcid0000-0001-9987-7301-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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