Structure and absolute configuration of nyasol and hinokiresinol via synthesis and vibrational circular dichroism spectroscopy

J Nat Prod. 2005 Nov;68(11):1603-9. doi: 10.1021/np0502995.

Abstract

The absolute configuration of the norlignan (+)-nyasol was determined to be S by comparison of the experimental vibrational circular dichroism data with first-principle calculations taking into account the eight lowest energy conformations. The established absolute configuration of (+)-nyasol enables establishment of the absolute configuration of (-)-hinokiresinol, which is concluded to be S. A total synthesis and resolution of hinokiresinol has been performed to resolve the conflicting reports of the coupling constant of the vinylic protons of the disubstituted double bond in this molecule. Racemic hinokiresinol was resolved. Both enantiomers possess the same antiplasmodial activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimalarials / chemical synthesis
  • Antimalarials / chemistry*
  • Antimalarials / pharmacology
  • Circular Dichroism
  • Lignans / chemical synthesis
  • Lignans / chemistry*
  • Lignans / pharmacology
  • Molecular Structure
  • Phenols / chemical synthesis
  • Phenols / chemistry*
  • Phenols / pharmacology
  • Plasmodium falciparum / drug effects*
  • Stereoisomerism

Substances

  • Antimalarials
  • Lignans
  • Phenols
  • hinokiresinol
  • nyasol