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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Krishnan, V S H | - |
| dc.contributor.author | Chowdary, K S | - |
| dc.contributor.author | Dubey, P K | - |
| dc.date.accessioned | 2013-03-30T17:27:55Z | - |
| dc.date.available | 2013-03-30T17:27:55Z | - |
| dc.date.issued | 1999-12 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16675 | - |
| dc.description | 1371-1373 | en_US |
| dc.description.abstract | Attempted dehydrogenative cyclisation of 2-chloro-3-(2 'benzylidinehydrazino) quinoxaline 5 with a view to prepare 1-phenyl-4-chloro[1,2,4] triazolo [4,3-a] quinoxaline 6 using cupric acetate gives l-phenyl-4-oxo-[1,2,4]triazolo[4,3-a]quinoxaline 7. A rational explanation is offered for this reaction and the applicability of cupric acetate as dehydrogenative cyclisation agent (such as in the conversion of 10→11) has been demonstrated. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.38B(12) December 1999] | en_US |
| dc.title | Formation of 1-phenyl-4-oxo [1,2,4] triazolo[ 4,3-a]quinoxaline from 2-chloro-3-(2' -benzylidenehydrazino)quinoxaline during dehydrogenative cyclisation using cupric acetate | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(12) December 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(12) 1371-1373.pdf | 630.72 kB | Adobe PDF | View/Open |
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