Total Synthesis of Lyconesidine B, a Lycopodium Alkaloid with an Oxygenated, Amine-Type Fawcettimine Core

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This report describes the total synthesis of the complex, oxygenated tetracyclic alkaloid, lyconesidine B. The key synthetic challenge involves diastereoselective generation of a decahydroquinoline ring with a quaternary carbon at the angular position via domino cyclopropanation, ring-opening, and reduction. Another crucial step is the domino ene-yne metathesis involving a quaternary ammonium ion, leading to the construction of a decahydroazaazulen framework.

収録刊行物

  • Organic Letters

    Organic Letters 23 (3), 676-681, 2021-02

    American Chemical Society (ACS)

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詳細情報 詳細情報について

  • CRID
    1050571948037518720
  • NII論文ID
    120007177779
  • ISSN
    15237052
    15237060
  • HANDLE
    2433/266607
  • 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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