Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/8275| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Melo, Teresa M. V. D. Pinho e | - |
| dc.date.accessioned | 2009-02-09T14:32:14Z | - |
| dc.date.available | 2009-02-09T14:32:14Z | - |
| dc.date.issued | 2006 | en_US |
| dc.identifier.citation | European Journal of Organic Chemistry. 2006:13 (2006) 2873-2888 | en_US |
| dc.identifier.uri | https://hdl.handle.net/10316/8275 | - |
| dc.description.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) | en_US |
| dc.language.iso | eng | eng |
| dc.rights | openAccess | eng |
| dc.title | Conjugated Azomethine Ylides | en_US |
| dc.type | article | en_US |
| dc.identifier.doi | 10.1002/ejoc.200500892 | en_US |
| uc.controloAutoridade | Sim | - |
| item.grantfulltext | open | - |
| item.fulltext | Com Texto completo | - |
| item.openairetype | article | - |
| item.languageiso639-1 | en | - |
| item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
| item.cerifentitytype | Publications | - |
| crisitem.author.researchunit | CQC - Coimbra Chemistry Centre | - |
| crisitem.author.parentresearchunit | Faculty of Sciences and Technology | - |
| crisitem.author.orcid | 0000-0003-3256-4954 | - |
| Appears in Collections: | FCTUC Química - Artigos em Revistas Internacionais | |
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