Synthesis of Dibenzopyranones through Palladium‐Catalyzed Directed C–H Activation/Carbonylation of 2‐Arylphenols
- 12 August 2013
- journal article
- research article
- Published by Wiley in Angewandte Chemie
- Vol. 52 (40), 10598-10601
- https://doi.org/10.1002/anie.201304295
Abstract
Dibenzopyranones were synthesized by a palladium‐catalyzed phenol‐directed C–H activation/carbonylation of 2‐phenylphenol derivatives in the presence of CO. Pd(OAc)2 was used as a catalyst and Cu(OAc)2 as a catalytic oxidant in the presence of air.This publication has 57 references indexed in Scilit:
- Pd-Catalyzed C–H Lactonization for Expedient Synthesis of Biaryl Lactones and Total Synthesis of CannabinolOrganic Letters, 2013
- Synthesis of phenanthridinones viapalladium-catalyzed C(sp2)–H aminocarbonylation of unprotected o-arylanilinesChemical Communications, 2013
- Weak Coordination as a Powerful Means for Developing Broadly Useful C–H Functionalization ReactionsAccounts of Chemical Research, 2011
- Rhodium Catalyzed Chelation-Assisted C–H Bond Functionalization ReactionsAccounts of Chemical Research, 2011
- Palladium-catalyzed carbonylative coupling reactions between Ar–X and carbon nucleophilesChemical Society Reviews, 2011
- Pd(II)-Catalyzed Carbonylation of C(sp3)−H Bonds: A New Entry to 1,4-Dicarbonyl CompoundsJournal of the American Chemical Society, 2010
- Palladium-Catalyzed Ligand-Directed C−H Functionalization ReactionsChemical Reviews, 2010
- Palladium- and Copper-Catalyzed Arylation of Carbon−Hydrogen BondsAccounts of Chemical Research, 2009
- Room‐Temperature Palladium‐Catalyzed C-H Activation: ortho‐Carbonylation of Aniline DerivativesAngewandte Chemie, 2009
- The Synthesis of Substituted Benzo[c]chromen‐6‐ones by a Suzuki Coupling and Lactonization Sequence Using Ionic Liquids – from Laboratory Scale to Multi‐Kilogram SynthesisEuropean Journal of Organic Chemistry, 2006