• Title of article

    Stereoselective synthesis of the right-hand segment of tubiferal A

  • Author/Authors

    Hiramatsu، نويسنده , , Takahiro and Takahashi، نويسنده , , Motomasa and Tanino، نويسنده , , Keiji، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2014
  • Pages
    3
  • From page
    1145
  • To page
    1147
  • Abstract
    Tubiferal A, a triterpenoid isolated from myxomycete Tubifera dimorphotheca, exhibits a reversal effect of vincristine (VCR) resistance against VCR-resistant KB cell lines. The compound possesses a complex structure involving the 6-7-6-5 polycyclic carbon framework with various functional groups. The stereoselective synthesis of the right-hand segment of tubiferal A was achieved on the basis of the cyclopentene annulation method and the semi-pinacol rearrangement reaction of an epoxy alcohol for constructing the trans-fused 6-5 bicyclic skeleton possessing two quaternary carbon atoms at the angular positions.
  • Keywords
    Semi pinacol rearrangement , Hydrindane skeleton , Tubiferal A , total synthesis
  • Journal title
    Tetrahedron Letters
  • Serial Year
    2014
  • Journal title
    Tetrahedron Letters
  • Record number

    1888138