A Novel and Efficient One Pot Synthesis of 2,4-Disubstituted Thiazoles and Oxazoles Using Phenyltrimethylammoniumtribromide in Ionic Liquid

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dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-27T04:09:41Z
dc.date.available2021-10-27T04:09:41Z
dc.date.issued2012-09-10
dc.description.abstractA novel and efficient one-pot procedure has been described for synthesis of 2,4-disubstituted thiazoles and oxazoles from substituted ketones using phenyltrimethylammoniumtribromide as in situ brominating agent followed by reaction with thioamide/thiourea and amides/ureas, respectively in [bmim][BF4] ionicliquid. The advantages of the procedure include avoiding the handling of lacrymetric compounds, hazardous and toxic organic solvents along with good to excellent yield of the products.en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1002/jhet.904?jhet904-eo-0005=
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2919
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectThiazolesen_US
dc.subjectOxazolesen_US
dc.subjectPhenyltrimethylammoniumtribromideen_US
dc.titleA Novel and Efficient One Pot Synthesis of 2,4-Disubstituted Thiazoles and Oxazoles Using Phenyltrimethylammoniumtribromide in Ionic Liquiden_US
dc.typeArticleen_US

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