Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/16523
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dc.contributor.authorMallik, Asok K-
dc.contributor.authorChattopadhyay, Falguni-
dc.date.accessioned2013-03-27T20:11:49Z-
dc.date.available2013-03-27T20:11:49Z-
dc.date.issued1999-08-
dc.identifier.urihttp://hdl.handle.net/123456789/16523-
dc.description889-892en_US
dc.description.abstractOn treatment with NaN3/TFA, some E-3-benzylideneflavanones yield 3-benwylchromones with the loss of 2-aryl group as the corresponding aniline, a plausible mechanistic path for which has been delineated. An acid-catalysed skeletal rearrangement of some E-3-benzylideneflavanones also takes place.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(08) [August 1999]en_US
dc.titleNovel conversion of some E-3-benzylideneflavanones to 3-benzoylchromones under a Schmidt rearrangement conditionen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(08) [August 1999]

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