Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/5078
Title: 1,3-Dipolar cycloaddition of azomethine ylides generated from aziridines in supercritical carbon dioxide
Authors: Gomes, Paulo J. S. 
Nunes, Cláudio M. 
Pais, Alberto A. C. C. 
Melo, Teresa M. V. D. Pinho e 
Arnaut, Luis G. 
Keywords: Supercritical carbon dioxide; 1,3-Dipolar cycloaddition; Azomethine ylides; Aziridines
Issue Date: 2006
Citation: Tetrahedron Letters. 47:31 (2006) 5475-5479
Abstract: The 1,3-dipolar cycloaddition of azomethine ylides with DMAD in supercritical carbon dioxide is reported. The photolysis reaction conditions were optimized with a suitable adjustment of pressure, temperature, irradiation time and co-solvent concentration leading to a more efficient reaction than in neat acetonitrile. Similar results were observed using thermal reaction conditions. Supercritical carbon dioxide with a minute co-solvent addition is shown to be a very efficient medium for promoting this type of cycloadditions.
URI: http://hdl.handle.net/10316/5078
DOI: 10.1016/j.tetlet.2006.05.179
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

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