Abstract <p>Novel optically active thioethers and sulfones based on 2(5<i>H</i>)-furanone, 4-aminothiophenol, and two monoterpene alcohols <i>l</i>-menthol and <i>l</i>-borneol are synthesized. The crystal structures of two optically active sulfonyl derivatives of the furanone series are studied by single crystal X-ray diffraction (XRD). In both crystals, the compound is presented by independent molecules A and B having radical differences in conformations and hydrogen bond systems. The efficiency of the approach involving a detailed examination of all stereochemical features of a molecule in a crystal is demonstrated based on single crystal XRD data with the use of the Hirshfeld surface analysis.</p>

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Crystal Structure of Optically Active Sulfones Based on 4-Aminothiophenol and 5-Menthyloxy- and 5-Bornyloxy-2(5H)-Furanones: Stereochemical Features

  • D. P. Gerasimova,
  • L. V. Frantsuzova,
  • A. F. Saifina,
  • A. M. Khabibrakhmanova,
  • A. M. Khabibullina,
  • E. S. Rabbanieva,
  • A. R. Kurbangalieva,
  • O. A. Lodochnikova

摘要

Abstract

Novel optically active thioethers and sulfones based on 2(5H)-furanone, 4-aminothiophenol, and two monoterpene alcohols l-menthol and l-borneol are synthesized. The crystal structures of two optically active sulfonyl derivatives of the furanone series are studied by single crystal X-ray diffraction (XRD). In both crystals, the compound is presented by independent molecules A and B having radical differences in conformations and hydrogen bond systems. The efficiency of the approach involving a detailed examination of all stereochemical features of a molecule in a crystal is demonstrated based on single crystal XRD data with the use of the Hirshfeld surface analysis.