Article ID Journal Published Year Pages File Type
9614512 Journal of Molecular Catalysis A: Chemical 2005 6 Pages PDF
Abstract
Two flexible bis-triarylphosphine chelators based on a calix[4]arene scaffold were assessed in combination with Pd or Ni as catalysts for CC bond forming reactions involving aryl halides. Both ligands resulted in efficient catalysts for Heck, Suzuki and Kumada-Corriu cross-coupling reactions. The diphosphines were shown to be superior to PPh3 when chlorobenzene was used as reagent.
Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
Authors
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