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Synthetic Approach and Structural Characterization of Acetyl-Protected α-D-Glucosyl 1,2,4-Dithiazolidines

Author

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  • Abhijit C. Shahu
  • Santosh B. Gaikwad
  • Kishore Puri

Abstract

The reaction of N-glucose-S-chloroisothiocarbamoyl chloride with different ammonium aryl dithiocarbamates made a number of unique 3-thio-4-acetyl-α-D-glucosyl-5-arylimino-1,2,4-dithiazolidines. The synthetic process can be used to make N-glucoside derivatives that have the 1,2,4-dithiazolidine framework in a way that works well. We figured out the structures of the compounds we made by using both traditional chemical transformations and spectroscopic methods. These methods were mass spectrometry, infrared (IR) spectroscopy, and proton nuclear magnetic resonance (¹H NMR). The combined spectrum data showed that the newly made glucosyl dithiazolidine derivatives had successfully formed and kept their structural integrity.

Suggested Citation

  • Abhijit C. Shahu & Santosh B. Gaikwad & Kishore Puri, 2026. "Synthetic Approach and Structural Characterization of Acetyl-Protected α-D-Glucosyl 1,2,4-Dithiazolidines," International Journal of Scientific Research in Chemistry, International Journal of Scientific Research in Chemistry, vol. 11(2), pages 47-53, March.
    • Handle: RePEc:cuo:ijsrch:v11:y2026:i2:id:87
    DOI: 10.32628/IJSRCH261128
    Note: Article URL: https://ijsrch.com/home/article/view/IJSRCH261128
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