A Convenient Synthesis Of Pyrandione Derivatives Using P-toluenesulfonic Acid As Catalyst Under Ultrasound Irradiation

dc.contributor.authorBenosmane, N.
dc.contributor.authorBoutemeur, B.
dc.contributor.authorHamdi, S.m.
dc.contributor.authorHamdi, M.
dc.date.accessioned2020-10-28T10:18:42Z
dc.date.available2020-10-28T10:18:42Z
dc.date.issued2016-09-01
dc.descriptionArticale in Journal of fundamental and Applied Sciences Vol. 08, N. 03en_US
dc.description.abstractA new series of 3,3'-{alkane-α,ω-diylbis[imino-eth-1-yl-1-ylidene]}bis(6-methyl-2H-pyran- 2,4(3H)-dione) derivatives (3c-e) has been synthesized by the convenient ultrasound-mediated condensation of a diamine with dehydroacetic acid in the presence of a catalytic amount of p- toluenesulfonic acid. The structure of all synthesized compounds was elucidated by IR spectroscopy, 1H NMR spectroscopic spectra, elemental analysis, and mass spectroscopy. A tautomeric form for the derivatives species is also proposed.en_US
dc.identifier.citationArticale in Journal of fundamental and Applied Sciences Vol. 08, N. 03en_US
dc.identifier.issn1112-9867
dc.identifier.urihttp://dspace.univ-eloued.dz/handle/123456789/7347
dc.language.isoenen_US
dc.publisherUniversity of Eloued جامعة الواديen_US
dc.subjectDehydroacetic acid; Schiff base; Condensation; Catalyst; Ultrasound irradiation; Tautomerism.en_US
dc.titleA Convenient Synthesis Of Pyrandione Derivatives Using P-toluenesulfonic Acid As Catalyst Under Ultrasound Irradiationen_US
dc.typeArticleen_US

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