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dc.contributor.authorPonnusamy, S-
dc.contributor.authorPitchumani, K-
dc.date.accessioned2013-03-27T20:09:28Z-
dc.date.available2013-03-27T20:09:28Z-
dc.date.issued1999-07-
dc.identifier.urihttp://hdl.handle.net/123456789/16522-
dc.description861-864en_US
dc.description.abstractBeckmann rearrangement of acetone oxime, acetophenone oxime and benzophenone oxime has been studied in the presence of para-toluenesulphonic acid as a solid catalyst. The rearrangement is found to proceed smoothly and under milder conditions. It is observed that in the case of benzophenone oxime, elevated temperatures favour rearrangement, while deoximation is predominant at room temperature. An explanation is presented and the mechanism is discussed.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.38B(07) [July 1999]en_US
dc.titleFacile PTSH-catalysed Beckmann rearrangement of ketoximes in solid stateen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(07) [July 1999]

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