A novel green protocol for ligand free Suzuki–Miyaura cross-coupling reactions in WEB at room temperature
- 23 January 2015
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 17 (3), 1442-1445
- https://doi.org/10.1039/c4gc02522a
Abstract
A highly efficient green protocol for palladium acetate-catalysed ligand-free Suzuki–Miyaura cross-coupling reactions in neat ‘water extract of banana (WEB)’ was developed. Suzuki–Miyaura reaction proceeds in WEB at very short reaction times under ‘ligand/external base/external promoters/organic medium’ free conditions.This publication has 38 references indexed in Scilit:
- Palladiumkatalysierte Kreuzkupplungen: eine historische Perspektive im Kontext der Nobel‐Preise 2010Angewandte Chemie, 2012
- Nickel-Catalyzed Suzuki–Miyaura Reaction of Aryl FluoridesJournal of the American Chemical Society, 2011
- Efficient Synthesis of Sterically Crowded Biaryls by Palladium-Phosphinous Acid-Catalyzed Cross-Coupling of Aryl Halides and Aryl GrignardsThe Journal of Organic Chemistry, 2007
- Carbon−Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium CatalystsChemical Reviews, 2006
- Amino Alcohols as Ligands for Nickel-Catalyzed Suzuki Reactions of Unactivated Alkyl Halides, Including Secondary Alkyl Chlorides, with Arylboronic AcidsJournal of the American Chemical Society, 2006
- Rational Ligand Design in Constructing Efficient Catalyst Systems for Suzuki–Miyaura CouplingAngewandte Chemie, 2004
- Transition-Metal-Catalyzed Reactions in Heterocyclic SynthesisChemical Reviews, 2004
- Palladium-Catalyzed Coupling Reactions of Aryl ChloridesAngewandte Chemie, 2002
- NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic AcidsOrganic Letters, 2001
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995