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https://hdl.handle.net/10316/8275
Title: | Conjugated Azomethine Ylides | Authors: | Melo, Teresa M. V. D. Pinho e | 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) | URI: | https://hdl.handle.net/10316/8275 | DOI: | 10.1002/ejoc.200500892 | Rights: | openAccess |
Appears in Collections: | FCTUC Química - Artigos em Revistas Internacionais |
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