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
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
Journal title :
Tetrahedron Letters