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چکیده
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Electroorganic synthesis has considered as a valuable-powerful method for the development of environmentally friendly processes in the recent decades, this conception is because of lowenergy consumption and temperature, high selectivity, good atom economy, low costs for reagents, and moreover, electrons are considering as clean reagents too. Hydroquinone (HQ) is a natural ingredient in many agricultural products, such as vegetables, fruits and grains which is widely using as a reducing agent, antioxidant, polymerization inhibitor and also over-thecounter drugs such as skin lighteners. The p-benzoquinone which is the oxidized form of HQ is very reactive and can be attacked by variety of nucleophiles. Generally 1,3,4-thiadiazole derivatives are the well-known five-membered heterocycles which displaying a broad spectrum of biological activities such as antioxidant, antimicrobial, anti-inflammatory, antituberculosis, anticonvulsants, and anxiolytic. The focus of this study is on 2-Amino-5-mercapto-1,3,4- thiadiazole (AMT) which is a highly reactive molecule. The nucleophilic property of AMT which resulted from two active groups of amine and thiol made us to involve it in a Michael
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