Abstract:A simple and efficient preparation of novel series of mono-and bis-pyrrolidine-2,5-diones containing sulfonamide moiety was described. The strategy involved sequential one-pot sulfonylation-nucleophilic substitution procedure and was found effective under ultrasound activation and used for the first time. This approach allows the synthesis of products in good to excellent yields in short reaction time.
Organosulfur compounds have a pivotal role in the functionalities of many natural products, pharmaceuticals and organic materials. For these reason, the search for new methodologies for the formation of carbon–sulfur...
Organosulfur compounds have a pivotal role in the functionalities of many natural products, pharmaceuticals and organic materials. For these reason, the search for new methodologies for the formation of carbon–sulfur...
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