Facile Synthesis of Thiazolidin-4-one Derivatives Incorporating Indole Moiety

dc.contributor.authorA. Altamamy, Hussein.
dc.date.accessioned2017-11-27T07:51:25Z
dc.date.available2017-11-27T07:51:25Z
dc.date.issued2013
dc.description.abstractCondensation of ethyl 3-formyl-1H-indole-2-carboxylate (1) with thiosemicarbazide in ethanol gave ethyl 3-(thiosemicarbazidomethyl)-1H-indole-2-carboxylate (2). Treatment of 2 with chloroacetic acid afforded the thiazolidin-4-one derivative 3. Condensation of 3 with aromatic aldehydes gave the corresponding arylidene derivatives 4a-c. Cyclization of 4a-c with hydroxylamine hydrochloride in the presence of sodium acetate yielded thiazolidino[4,5-c]isoxazoline derivatives 5a-c. The structure of the synthesized compounds were confirmed using elemental and spectroscopic analysis.ar
dc.identifier.urihttps://repository.sebhau.edu.ly/handle/1/155
dc.language.isoenar
dc.publisherSebha Universityar
dc.titleFacile Synthesis of Thiazolidin-4-one Derivatives Incorporating Indole Moietyar
dc.typeArticlear
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