Sodium-Metal-Promoted Reductive 1,2-<i>syn</i>-Diboration of Alkynes with Reduction-Resistant Trimethoxyborane

  • 伊藤, 詩織
    Department of Chemistry, Graduate School of Science, Kyoto University
  • 深澤, 瑞喜
    Department of Chemistry, Graduate School of Science, Kyoto University
  • 高橋, 郁也
    Department of Chemistry, Graduate School of Science, Kyoto University
  • 野木, 馨介
    Department of Chemistry, Graduate School of Science, Kyoto University
  • 依光, 英樹
    Department of Chemistry, Graduate School of Science, Kyoto University

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タイトル別名
  • Sodium-metal-promoted reductive 1,2-syn-diboration of alkynes with reduction-resistant trimethoxyborane

抄録

Reductive 1, 2-diboration of alkynes has been accomplished by means of sodium dispersion in the presence of trimethoxyborane as a reduction-resistant boron electrophile. Two boron moieties can be introduced onto alkynes with excellent syn selectivity to afford the corresponding (Z)-1, 2-diborylalkenes. Bis(borate) species generated in situ can be involved in one-pot Suzuki-Miyaura arylation, formal arylboration of alkynes thus being executed.

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