Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/8275
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dc.contributor.authorMelo, Teresa M. V. D. Pinho e-
dc.date.accessioned2009-02-09T14:32:14Z-
dc.date.available2009-02-09T14:32:14Z-
dc.date.issued2006en_US
dc.identifier.citationEuropean Journal of Organic Chemistry. 2006:13 (2006) 2873-2888en_US
dc.identifier.urihttps://hdl.handle.net/10316/8275-
dc.description.abstractThe 1,3-dipolar cycloaddition of azomethine ylides is an efficient and versatile tool for the construction of five-membered nitrogen-heterocycles. When the azomethine ylide is conjugated with a double bond or a 1,3-diene moiety, other reactivity pathways are also available, namely 1,5-electrocyclization or 1,7-electrocyclization. The present review is focused on the generation and reactivity of this type of dipoles, which offer general strategies for the formation of five- and seven-membered nitrogen-heterocyclic compounds. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)en_US
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titleConjugated Azomethine Ylidesen_US
dc.typearticleen_US
dc.identifier.doi10.1002/ejoc.200500892en_US
uc.controloAutoridadeSim-
item.languageiso639-1en-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-3256-4954-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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