Ortho Arylation of Acetanilides via Pd(II)-Catalyzed C−H Functionalization

Related Content

• Highly Selective C−H Functionalization/Halogenation of Acetanilide Highly Selective C−H Functionalization/Halogenation of AcetanilideJournal of the American Chemical Society

  • Highly Selective C−H Functionalization/Halogenation of Acetanilide Highly Selective C−H Functionalization/Halogenation of Acetanilide

    Xiaobing Wan, Zhongxun Ma, Bijie Li, Keya Zhang, Shaokui Cao, Shiwei Zhang, and Zhangjie Shi
    Journal of the American Chemical Society 2006 128 (23), pp 7416–7417

    Abstract: Highly regioselective C−H functionalization/halogenation of acetanilides to produce ortho-haloacetanilides was catalyzed by Pd(OAc)₂ and Cu(OAc) ₂ with CuX₂ as the halogen source.

    Abstract | Full Text HTML | Hi-Res PDF
• Iridium-Catalyzed Addition of Acid Chlorides to Terminal AlkynesJournal of the American Chemical Society

  • Iridium-Catalyzed Addition of Acid Chlorides to Terminal Alkynes

    Tomohiro Iwai, Tetsuaki Fujihara, Jun Terao and Yasushi Tsuji
    Journal of the American Chemical Society 2009 131 (19), pp 6668–6669

    Abstract: An iridium N-heterocyclic carbene (NHC) complex, IrCl(cod)(IPr), successfully catalyzed an addition of common aromatic acid chlorides to terminal alkynes to afford (Z)-β-chloro-α,β-unsaturated ketones regio- and stereoselectively. When the NHC ligand (IPr)...

    Abstract | Full Text HTML | PDF w/ Links | Hi-Res PDF
• Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct ArylationChemical Reviews

  • Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation

    Dino Alberico, Mark E. Scott, and Mark Lautens
    Chemical Reviews 2007 107 (1), pp 174–238
    Abstract | Full Text HTML | Hi-Res PDF

Other ACS content by these authors:

• Shangdong Yang
• Bijie Li
• Xiaobing Wan
• Zhangjie Shi