Assignment of the absolute configuration of zwitterionic and neutral macropodumines by means of TDDFT CD calculations

Chirality. 2009 Jun;21(6):561-8. doi: 10.1002/chir.20626.

Abstract

Macropodumines B and C (1, 2) are fused pentacyclic alkaloids previously isolated from the Chinese medicinal plant Daphniphyllum macropodum. Macropodumine B (1) possesses an amazing structural feature of a cyclopentadienyl carbanion, stabilized as a zwitterion by an internal iminium cation, which was confirmed by X-ray diffraction analysis. On the basis of the X-ray geometry, the absolute configuration of 1 was determined by employing the solid-state CD/TDDFT approach. The absolute configuration of 2 was instead determined by using TDDFT CD calculations on DFT-optimized geometries, in comparison with CD spectra recorded in solution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Circular Dichroism
  • Crystallography, X-Ray
  • Models, Molecular
  • Molecular Conformation
  • Polycyclic Compounds / chemistry*
  • Quantum Theory*
  • Time Factors

Substances

  • Polycyclic Compounds
  • macropodumine B
  • macropodumine C