Synthesis of S-aryl dithiocarbamates and its in-silico studies

IF 4.2 Q2 CHEMISTRY, MULTIDISCIPLINARY Results in Chemistry Pub Date : 2025-05-01 Epub Date: 2025-04-09 DOI:10.1016/j.rechem.2025.102257
Krishnarao Jayaram Desai , Murugesan Santhosh , Padmanaban Akashvarunan , Ponraj Abarna , Boopathi Shagunthala Hariprasad , Sundaram Ganesh Babu , Annamalai Pratheepkumar
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Abstract

Environmentally friendly facile synthesis of aryl dithiocarbamates via a one-pot procedure by the reaction between secondary amines and carbon disulphide produced dithiocarbamates, which underwent copper-assisted intermolecular CS cross-coupling with aryl Iodides are developed. Cu2O is employed as a catalyst and water used as a green solvent, owing to their high reaction efficiency and benign reaction conditions in the context of green chemistry. We demonstrated detailed studies of possible intermediates, product diversification, and in-silico properties for some of the novel S-Aryl dithiocarbamates. Further, the compound 3cg possess good binding affinity towards alpha-amylase protein in comparison with Metformin.

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S-芳基二硫代氨基甲酸盐的合成及其硅内研究
研究了仲胺与二硫化碳一锅反应制备芳基二硫代氨基甲酸酯的方法,并将其与芳基碘化物进行铜辅助的分子间CS交联。在绿色化学背景下,以Cu2O为催化剂,水为绿色溶剂,反应效率高,反应条件良好。我们展示了一些新型s -芳基二硫代氨基甲酸酯可能的中间体,产品多样化和硅性能的详细研究。与二甲双胍相比,化合物3cg对α -淀粉酶蛋白具有良好的结合亲和力。
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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