Reaction of the catalyst 1 or Pd(OAc)2 with tetrabutylammonium acetate, dissolved in tetrabutylammonium bromide, leads to a fast formation of Pd nanoparticles which efficiently catalyze the stereospecific reaction of cinnamates with aryl halides to give â-aryl-substituted cinnamic esters. The role of tetrabutylammonium acetate is crucial in determining the formation of nanoparticles and stereospecificity of the C-C coupling process.

Pd Nanoparticles Catalyzed Stereospecific Synthesis of beta-Aryl Cinnamic Esters in Ionic Liquids

NACCI, Angelo;MONOPOLI A;CIOFFI, NICOLA
2003-01-01

Abstract

Reaction of the catalyst 1 or Pd(OAc)2 with tetrabutylammonium acetate, dissolved in tetrabutylammonium bromide, leads to a fast formation of Pd nanoparticles which efficiently catalyze the stereospecific reaction of cinnamates with aryl halides to give â-aryl-substituted cinnamic esters. The role of tetrabutylammonium acetate is crucial in determining the formation of nanoparticles and stereospecificity of the C-C coupling process.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/41142
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