Structural revision of stemoburkilline from an E-alkene to a Z-alkene

J Nat Prod. 2009 Feb 27;72(2):316-8. doi: 10.1021/np800755p.

Abstract

Semisynthesis studies starting from (11Z)-1',2'-didehydrostemofoline (4) indicated that the known Stemona alkaloid stemoburkilline is the Z-isomer and not the E-isomer as initially reported. The semisynthesis involved conversion of (11Z)-1',2'-didehydrostemofoline (4) to 11(S),12(S)-dihydrostemofoline (3) followed by a stereoselective base-catalyzed ring-opening reaction to give (Z)-stemoburkilline (8). The same product was obtained using a similar synthetic protocol starting from isostemofoline (6) via a based-catalyzed ring-opening reaction of 11(S),12(R)-dihydrostemofoline (1). A re-examination of the crude root extracts of Stemona burkillii Prain and further NOE studies established stemoburkilline as the Z-isomer (8).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemistry*
  • Alkenes / chemistry*
  • Furans / chemistry*
  • Heterocyclic Compounds, 4 or More Rings / chemistry*
  • Molecular Structure
  • Stemonaceae / chemistry*
  • Stereoisomerism

Substances

  • 11(S),12(R)-dihydrostemofoline
  • Alkaloids
  • Alkenes
  • Furans
  • Heterocyclic Compounds, 4 or More Rings
  • didehydrostemofoline
  • stemoburkilline