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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3110
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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:24:20Z-
dc.date.available2021-10-27T04:24:20Z-
dc.date.issued1996-
dc.identifier.urihttps://www.tandfonline.com/doi/abs/10.1080/00397919608004628-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3110-
dc.description.abstractReaction of 2-methylchromone (2) with phenylhydrazine provides 3-methyl-5-(o-hydroxyphenyl)-1-phenylpyrazole (6) as a major product. In contrast under similar conditions, heterocyclylhydrazines (8a-c) yield exclusively 5-ethyl-3-(o-hydroxyphenyl)-1-heterocyclylpyrazoles (9a-c). The structural assignments are based on an unambiguous synthesis and an analysis of NMR (1H & 13C) spectral data.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.subjectChemistryen_US
dc.subjectHeterocyclylhydrazinesen_US
dc.subject2-Methylchromoneen_US
dc.titleReaction of Aryl and Heterocyclylhydrazines with 2-Methylchromone: Structural Investigation of the Productsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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