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http://nopr.niscpr.res.in/handle/123456789/59338Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | B, Ranade Prasanna | - |
| dc.contributor.author | N, Navale Dinesh | - |
| dc.contributor.author | W, Zote Santosh | - |
| dc.contributor.author | K, Patil Digambar | - |
| dc.date.accessioned | 2022-03-23T10:03:10Z | - |
| dc.date.available | 2022-03-23T10:03:10Z | - |
| dc.date.issued | 2022-03 | - |
| dc.identifier.issn | 2583-1321 (Online); 0019-5103 (Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/59338 | - |
| dc.description | 325-327 | en_US |
| dc.description.abstract | A synthesis of substituted benzo[e][1,3]oxazin-4-one analogs has been carried out by two methods. One of the common procedures involves refluxing in situ generated imine with salicylic acid while other method involves one-pot three component condensation reaction between aldehyde, amine and salicylic acid using DCC. The synthesized compounds have been characterized by IR, 1H and 13C NMR spectroscopy. Melting points reported are uncorrected. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | NIScPR-CSIR, India | en_US |
| dc.source | IJC Vol.61(03) [March 2022] | en_US |
| dc.subject | Cyclisation | en_US |
| dc.subject | Schiff base | en_US |
| dc.subject | salicylic acid | en_US |
| dc.subject | DCC | en_US |
| dc.subject | benzo[e][1,3] oxazines | en_US |
| dc.title | Synthesis of substituted benzo[e][1,3]oxazino analogs | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC Vol.61(03) [March 2022] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Indian J Chem, 61, 325-327 (Mar,2022).pdf | Main Article | 2.95 MB | Adobe PDF | View/Open |
| Indian J Chem, 61, 325-327 (Mar,2022) Suppl. Data.pdf | Supplementary Data | 213.79 kB | Adobe PDF | View/Open |
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