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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T11:02:01Z-
dc.date.available2021-11-11T11:02:01Z-
dc.date.issued2011-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/00397910903576677-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3388-
dc.description.abstractAzaphenothiazine catalyses the intramolecular cyclization of N-(bromoalkyl)phthalimides in the presence of anhydrous K2CO3 to form spiro cyclic quaternary ammonium salts, namely azoniaspiro compounds, under microwave irradiation. A novel and ecofriendly method was developed for the synthesis of azoniaspiro compounds, and the role of azaphenothiazine as a catalyst in such reactions has been established for the first time. In the future, this protocol can be extended to the synthesis of various substituted N-heterocycles by hydrolyzing the resulting azoniaspiro compounds.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.subjectChemistryen_US
dc.subjectAzaphenothiazineen_US
dc.subjectAzoniaspiroen_US
dc.subjectCatalysten_US
dc.titleMicrowave-Assisted Synthesis of Azoniaspiro Compounds Using a Novel Catalyst, 1-Azaphenothiazineen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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