Synthetic studies of salinosporamide A through the intramolecular hydroamidation of alkynes

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Rhodium-catalyzed intramolecular hydroamidation of alkynes was carried out to construct the synthetic intermediates of a proteasome inhibitor, salinosporamide A. Several alkynyl formamides were synthesized and subjected to the hydroamidation reaction. Some derivatives with a methoxymethyl (MOM) or 2-methoxy-2-propyl (MOP) group near the reaction site were converted to the corresponding lactams in excellent yields.

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詳細情報 詳細情報について

  • CRID
    1050282677278147712
  • NII論文ID
    120002709543
  • NII書誌ID
    AA00704122
  • ISSN
    0022328X
  • HANDLE
    2433/134562
  • 本文言語コード
    en
  • 資料種別
    journal article
  • データソース種別
    • IRDB
    • CiNii Articles

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