A comparative study of hydroxyl- and carboxylate-functionalized imidazolium and benzimidazolium salts as precursors for N-heterocyclic carbene ligands
Contribuinte(s) |
Universidad de Alicante. Departamento de Química Orgánica Universidad de Alicante. Instituto Universitario de Síntesis Orgánica Nuevos Materiales y Catalizadores (MATCAT) |
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Data(s) |
15/09/2016
15/09/2016
01/09/2015
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Resumo |
The preparation of imidazolium and benzimidazolium salts with hydroxyl or carboxylate functions has been achieved using straightforward synthetic pathways. These salts in combination with palladium(II) acetate give active catalytic systems for Suzuki reaction. A comparative study has been performed, which has revealed that both the heterocycle and the functional group are important for the catalytic activity and stability of the catalyst. Financial support from the University of Alicante (VIGROB-285) and the Spanish Ministerio de Economía y Competitividad (CTQ2011-24165) is acknowledged. |
Identificador |
Applied Organometallic Chemistry. 2015, 29(9): 624-632. doi:10.1002/aoc.3343 0268-2605 (Print) 1099-0739 (Online) http://hdl.handle.net/10045/57940 10.1002/aoc.3343 |
Idioma(s) |
eng |
Publicador |
John Wiley & Sons |
Relação |
http://dx.doi.org/10.1002/aoc.3343 |
Direitos |
© 2015 John Wiley & Sons, Ltd. info:eu-repo/semantics/openAccess |
Palavras-Chave | #N-heterocyclic carbenes #Imidazolium #Benzimidazolium #Palladium #Suzuki–Miyaura #Química Orgánica |
Tipo |
info:eu-repo/semantics/article |