Gelsemine: a thought-provoking target for total synthesis

Angew Chem Int Ed Engl. 2003 Jan 3;42(1):36-51. doi: 10.1002/anie.200390048.

Abstract

Gelsemine and 21-oxogelsemine have been synthesized through several routes. This Review focuses on the comparison of the different strategies to assemble the bicyclo[3.2.1]octane core, to introduce the bridgehead quaternary C20 to form the pyrrolidine moiety, to construct the oxindole residue, and to close the tetrahydropyran ring en route to gelsemine.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alkaloids / chemical synthesis*
  • Alkaloids / chemistry
  • Cyclization
  • Gelsemium / chemistry
  • Molecular Structure
  • Photochemical Processes

Substances

  • Alkaloids
  • gelsemine