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Ionic and covalent copper(II)-based catalysts for Michael additions. The mechanism
Authors:Comelles Josep  Moreno-Mañas Marcial  Pérez Elisabet  Roglans Anna  Sebastián Rosa M  Vallribera Adelina
Institution:Department of Chemistry, Universitat Autonoma de Barcelona, Cerdanyola, 08193-Barcelona, Spain.
Abstract:Cu(SbF6)2-AdamBox and copper(II) bis-(5-tert-butylsalicylaldehydate) catalyze the Michael addition in neutral media. Mechanistic studies, based on UV-vis, IR, and electrospray ionization mass spectrometry (ESI-MS), suggest that copper enolates of the beta-dicarbonyl formed in situ are the active nucleophilic species.
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