University of Jiroft | Abdollah Ramazani

Research

Title	Unexpected regio‑ and stereoselective [4+3] cycloaddition reaction of azomethine ylides with benzylidene thiazolidinediones: synthesis of pharmacologically active spiroindoline oxazepine derivatives and theoretical study
Type	Article
Keywords	Regioselectivity · Spiroindoline oxazepine · [4+3] Cycloaddition reaction · Pharmacologically active · Theoretical NMR analysis
Researchers	Mahboobeh Zahedifar, Behjat Pouramiri, Fereshteh Ezzatighadi, razieh razavi, Abdollah Ramazani

Abstract

An unexpected regio- and stereoselective [4+3] cycloaddition reaction of azomethine ylides with 5-benzylidenethiazolidine-2,4-diones has been successfully developed for the synthesis of the novel pharmacologically active 4′,5′-dihydro-3′Hspiro[indoline-3,2′-[1, 3] oxazepin]-2-one derivatives in basic condition. Easy purifcation, high yield, short experimental time and operational simplicity are specifc advantages of this protocol. Furthermore, all the synthesized compounds have been evaluated for antioxidant and antibacterial activities. According to the results, most of the synthesized compounds exhibited DPPH radical scavenging activity and nine of them showed antibacterial properties. The reaction mechanism and 1 H NMR spectrum have been evaluated by B3LYP/6311G method.