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

Abhijit C. Shahu, Santosh B. Gaikwad and Kishore Puri

International Journal of Scientific Research in Chemistry, 2026, vol. 11, issue 2, 47-53

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.

Keywords: N-glucoside; dithiocarbamates; glucosyl dithiazolidine; acetyl derivatives; carbohydrates (search for similar items in EconPapers)
Date: 2026
Note: Article URL: https://ijsrch.com/home/article/view/IJSRCH261128
References: Add references at CitEc
Citations:

Downloads: (external link)
https://ijsrch.com/home/article/view/IJSRCH261128 Article URL (text/html)
https://ijsrch.com/home/article/download/IJSRCH261128/IJSRCH261128 Full text (application/pdf)

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:cuo:ijsrch:v11:y2026:i2:id:87

DOI: 10.32628/IJSRCH261128

Access Statistics for this article

More articles in International Journal of Scientific Research in Chemistry from International Journal of Scientific Research in Chemistry
Bibliographic data for series maintained by Pankaj Sharma ().