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Showing 1–7 of 7 results
Advanced filters: Author: Fanke Meng Clear advanced filters

  • Enantioenriched cyclobutenes and cyclobutanes are important units in medicinal chemistry, natural products and material science, and are useful intermediates in organic synthesis. Herein, the authors report a cobalt-catalyzed protocol for pathway-divergent enantioselective coupling of alkynes and cyclobutenes.

    • Jiwu Zhang
    • Meng Wu
    • Fanke Meng
    ResearchOpen Access
    Nature Communications
    Volume: 16, P: 1-14

  • The development of divergent reaction pathways controlled by different ligands is a critical goal. Here the authors describe a cobalt-catalyzed strategy for cascade coupling of 1,3-enynes with two molecules of acrylates through three reaction modes.

    • Heng Wang
    • Xiaofeng Jie
    • Fanke Meng
    ResearchOpen Access
    Nature Communications
    Volume: 15, P: 1-10

  • Catalytic enantioselective introduction of a propargyl group is an important carbon–carbon forming reactions but only few Cu- or Ni-catalyzed protocols with limited reaction modes are known. Here, the authors describe a photoredox/cobalt-catalyzed propargyl addition to aldehydes via propargyl radicals which enables the construction of a broad scope of homopropargyl alcohols.

    • Lei Wang
    • Chuiyi Lin
    • Fanke Meng
    ResearchOpen Access
    Nature Communications
    Volume: 14, P: 1-15

  • Plasmonic nanostructures may enhance solar energy collection. Here, the authors exploit both plasmon-induced resonant energy transfer and surface plasmon polaritons in a hematite–gold nano-array, leading to a tenfold increase in the photocurrent at a bias of 0.23 V in a photoelectrochemical cell.

    • Jiangtian Li
    • Scott K. Cushing
    • Nianqiang Wu
    Research
    Nature Communications
    Volume: 4, P: 1-8

  • A catalytic process is reported that begins with a highly selective copper–boron addition to a monosubstituted allene, and in which the resulting boron-substituted organocopper intermediate then participates in a chemoselective, site-selective and enantioselective allylic substitution; this approach is used in the enantioselective synthesis of gram quantities of two natural products.

    • Fanke Meng
    • Kevin P. McGrath
    • Amir H. Hoveyda
    Research
    Nature
    Volume: 513, P: 367-374