Please use this identifier to cite or link to this item: http://localhost:8081/jspui/handle/123456789/21349
Title: Synthesis of Benzylidene-phenylpyrrolidine-dione and Isoxazolone based Nitrogen Heterocycles and their Synthetic Transformations
Authors: Kumari, Ankita
Issue Date: Apr-2022
Publisher: IIT Roorkee
Abstract: Herein, we have demonstrated a greener approach for the synthesis of isoxazole-4-(5H)ones via a one-pot cyclocondensation reaction of aromatic aldehydes, hydroxylamine hydrochloride and ethyl acetoacetate in ethanol. This method afforded isoxazole-5-(4H)-ones in high yield. 3 Arylidene pyrrolidine-2,5-diones are good Michael acceptors and show Diels-Alder reactivity across the double bond. Herein, we have demonstrated the synthesis of 3-arylidene pyrrolidine 2,5-diones via reaction of N-phenyl maleimide with triphenylphosphine and the formed TPP maleimide adduct was reacted with benzaldehyde in ethanol to give (E)-3-arylmethylidene pyrrolidene-2,5-diones in excellent yield.
URI: http://localhost:8081/jspui/handle/123456789/21349
Research Supervisor/ Guide: Peddinti, RamaKrishna
metadata.dc.type: Dissertations
Appears in Collections:MASTERS' THESES (Chemistry)

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