Locascio Theresa M, Tunge Jon A
Department of Chemistry, The University of Kansas, 2010 Malott Hall, 1251 Wescoe Hall Drive, Lawrence, KS, 66045, USA.
Chemistry. 2016 Dec 12;22(50):18140-18146. doi: 10.1002/chem.201603481. Epub 2016 Oct 31.
The palladium(0)-catalyzed, ligand-controlled, regioselective addition of diaryl acetonitrile pronucleophiles to propargylic carbonates is reported. Selective formation of either terminal 1,3-dienyl or propargylated products is proposed to arise from a change in reaction mechanism controlled by the denticity of the coordinating ligand.
据报道,钯(0)催化、配体控制、区域选择性地将二芳基乙腈亲核前体加成到炔丙基碳酸酯上。据推测,通过改变由配位配体的齿数控制的反应机理,可以选择性地生成末端1,3-二烯基产物或炔丙基化产物。