Chiral Thianthrenes

Int J Mol Sci. 2024 Apr 13;25(8):4311. doi: 10.3390/ijms25084311.

Abstract

The absolute configuration and stability of two thianthrene chiral sulfoxides has been determined by means of X-ray single-crystal structure determinations. The analyses and configurations allow verification that the diastereomeric sulfoxides are stable in solution and are not interconverting, which has been suggested in some studies of sulfoxides. The two thianthrene sulfoxides have slightly different Rf values, which allowed their separation using flash chromatography on silica. The spots run back-to-back, which posed a challenge for their separation. The pure, separated compounds in solution remain as separate, single spots on a Thin Layer Chromatography (TLC) plate.

Keywords: chiral sulfoxide; configuration; diastereoisomer; dithiin; resolution; sulfoxide; thianthrene.

MeSH terms

  • Chromatography, Thin Layer / methods
  • Crystallography, X-Ray / methods
  • Models, Molecular
  • Molecular Structure
  • Phenanthrenes / chemistry
  • Stereoisomerism
  • Sulfoxides* / chemistry

Substances

  • Sulfoxides
  • Phenanthrenes

Grants and funding

The authors received no financial support for the research, authorship and/or publication of this article.