Stereoselective synthesis of the atropisomers of myristinin B/C

Org Lett. 2006 Apr 27;8(9):1925-7. doi: 10.1021/ol060511b.

Abstract

[reaction: see text] The first stereoselective synthesis of a potent DNA damaging agent, (-)-myristinin B/C, has been accomplished. This efficient synthesis allowed for unambiguous confirmation of the structure and absolute stereochemistry of the atropisomeric natural product. The antipode, (+)-myristinin B/C, was also synthesized, providing ample material for biological evaluation of both enantiomers.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • DNA Damage
  • Flavonoids / chemical synthesis*
  • Flavonoids / chemistry
  • Flavonoids / pharmacology
  • Molecular Structure
  • Stereoisomerism

Substances

  • Flavonoids
  • myristinin B
  • myristinin C