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http://nopr.niscpr.res.in/handle/123456789/6691Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Siddiqui, Zeba N | - |
| dc.contributor.author | Khuwaja, Gulrana | - |
| dc.contributor.author | Asad, M | - |
| dc.date.accessioned | 2009-11-19T10:07:10Z | - |
| dc.date.available | 2009-11-19T10:07:10Z | - |
| dc.date.issued | 2006-10 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/6691 | - |
| dc.description | 2341-2345 | en_US |
| dc.description.abstract | The nucleophilic character of triacetic acid lactone has been exploited here in the Michael condensation reaction involving 2-amino-3-formylchromone as the starting material. The reaction, as visualized, afforded yellow crystalline product 4. The compound has been characterized on the basis of spectral data and evaluated for antimicrobial activity | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int. Cl.8 C07D | en_US |
| dc.source | IJC-B Vol.45B(10) [October 2006] | en_US |
| dc.subject | Triacetic acid lactone | en_US |
| dc.subject | 3-acetoacetyl-5-oxo-5H-[1] benzopyrano [3,2-e] pyridin-2-one | en_US |
| dc.subject | antimicrobial activity | en_US |
| dc.subject | green chemistry | en_US |
| dc.title | One pot synthesis of 3-acetoacetyl-5-oxo-5H-[1] benzopyrano [3,2-e]pyridin-2-one from triacetic acid lactone | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.45B(10) [October 2006] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 45B(10) 2341-2345.pdf | 61.07 kB | Adobe PDF | View/Open |
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