Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/708Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Singh, Krishna Nand | - |
| dc.contributor.author | Kumar, Rajesh | - |
| dc.date.accessioned | 2008-04-03T11:32:42Z | - |
| dc.date.available | 2008-04-03T11:32:42Z | - |
| dc.date.issued | 2007-09 | - |
| dc.identifier.issn | 0376-4699 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/708 | - |
| dc.description | 1554-1557 | en_US |
| dc.description.abstract | A number of flavonoids have been allowed to react under the mild reaction conditions of tetraethylammonium superoxide in dry dimethylformamide at room temperature. As an outcome, 3-hydroxyflavones 1a-c undergo oxidative ring cleavage to afford 2-benzoyloxyphenylglyoxylic acids 2a-c, whereas the substrates 1d-f result in the formation of acids 2d-f alongwith 3d-f. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | IJCB Vol.46B(9) [September 2007] | en_US |
| dc.subject | Tetraethylammonium superoxide | en_US |
| dc.subject | Phase transfer catalyst | en_US |
| dc.subject | Flavonoids | en_US |
| dc.subject | Hydrophobic conditions | en_US |
| dc.title | Reactivity pattern of in situ generated tetraethylammoniun superoxide with some flavonoids | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.46B(09) [September 2007] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 46B(9) (2007) 1554-1557.pdf | 101.41 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.