Regioselective Hydrocarbamoylation of 1-Alkenes

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著者

    • MIYAZAKI Yosuke
    • Department of Material Chemistry, Graduate School of Engineering, Kyoto University
    • YAMADA Yuuya
    • Department of Material Chemistry, Graduate School of Engineering, Kyoto University
    • NAKAO Yoshiaki
    • Department of Material Chemistry, Graduate School of Engineering, Kyoto University

抄録

Nickel/Lewis acid cooperative catalysis derived from [Ni(cod)2], AlEt3, and N-heterocyclic carbene (NHC) effects highly regioselective hydrocarbamoylation of 1-alkenes. Variously substituted formamides and 1-alkenes can be employed to give a range of linear alkanamides regioselectively.

Nickel/Lewis acid cooperative catalysis derived from [Ni(cod)<sub>2</sub>], AlEt<sub>3</sub>, and <i>N</i>-heterocyclic carbene (NHC) effects highly regioselective hydrocarbamoylation of 1-alkenes. Variously substituted formamides and 1-alkenes can be employed to give a range of linear alkanamides regioselectively.

収録刊行物

  • Chemistry letters

    Chemistry letters 41(3), 298-300, 2012-03-05

    公益社団法人 日本化学会

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各種コード

  • NII論文ID(NAID)
    10030224504
  • NII書誌ID(NCID)
    AA00603318
  • 本文言語コード
    ENG
  • 資料種別
    SHO
  • ISSN
    03667022
  • データ提供元
    CJP書誌  IR  J-STAGE 
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