| dc.contributor.author | Kumar, Dalip | |
| dc.date.accessioned | 2021-10-27T04:24:20Z | |
| dc.date.available | 2021-10-27T04:24:20Z | |
| dc.date.issued | 1996 | |
| dc.identifier.uri | https://www.tandfonline.com/doi/abs/10.1080/00397919608004628 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3110 | |
| dc.description.abstract | Reaction 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.iso | en | en_US |
| dc.publisher | Taylor & Francis | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Heterocyclylhydrazines | en_US |
| dc.subject | 2-Methylchromone | en_US |
| dc.title | Reaction of Aryl and Heterocyclylhydrazines with 2-Methylchromone: Structural Investigation of the Products | en_US |
| dc.type | Article | en_US |
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