Selective Intermolecular [2+2+2] Cycloaddition of Terminal Alkynes and Alkenes by NbCl5 as a Catalyst Precursor

  • Kamei Motofumi
    Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University
  • Watanabe Keisuke
    Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University
  • Fuji Maito
    Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University
  • Obora Yasushi
    Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University

書誌事項

タイトル別名
  • Selective Intermolecular [2+2+2] Cycloaddition of Terminal Alkynes and Alkenes by NbCl<sub>5</sub> as a Catalyst Precursor

抄録

NbCl5 serves as an efficient catalyst for the intermolecular [2+2+2] cycloaddition of alkynes and alkenes to afford 1,3-cyclohexadienes. A convenient system has been developed using excess alkene, which enables the reaction to proceed without using low-valent niobium reagents or any reductants. This catalytic system affords 1,3-cyclohexadiene with high chemo- and regioselectivity, in contrast to a previously reported system involving NbCl3(DME) as a low-valent niobium catalyst.

収録刊行物

  • Chemistry Letters

    Chemistry Letters 45 (8), 943-945, 2016

    公益社団法人 日本化学会

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