Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16474
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dc.contributor.authorDubey, P K-
dc.contributor.authorKumar, R Vinod-
dc.date.accessioned2013-03-24T13:18:09Z-
dc.date.available2013-03-24T13:18:09Z-
dc.date.issued1999-06-
dc.identifier.urihttp://hdl.handle.net/123456789/16474-
dc.description732-734en_US
dc.description.abstractThe reaction of 2, 3-pyridinediamine 1a and its 5-bromo analogue 1b with 2-phenyl-3,1 -benzoxazin-4(H)-one 2 in refluxing acetic acid leads to the formation of 2-(2'-N-benzoylaminophenyl)imidazo[ 4. 5-b]pyridine 3a and 6-bromo-2-(2'-N-benzoylaminophenyl)imidazo[4, 5-b]pyridine 3b as products. A mechanistic pathway for the formation of 3 is described.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(06) [June 1999]en_US
dc.titleStudies on the condensation of 2, 3-pyridinediamines with 2-phenyl-3,1 -benzoxazin-4(H)-oneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(06) [June 1999]

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