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Title: Conjugated Azomethine Ylides
Authors: Melo, Teresa M. V. D. Pinho e 
Issue Date: 2006
Issue Date: 2006
Citation: European Journal of Organic Chemistry. 2006:13 (2006) 2873-2888
Abstract: The 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)
DOI: 10.1002/ejoc.200500892
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

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