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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Singal, Kewal Krishan | - |
| dc.contributor.author | Singh, Baldev | - |
| dc.date.accessioned | 2013-03-09T10:47:05Z | - |
| dc.date.available | 2013-03-09T10:47:05Z | - |
| dc.date.issued | 1999-03 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16308 | - |
| dc.description | 292-296 | en_US |
| dc.description.abstract | 1,3-Dipolar cycloaddition of substituted open-chain conjugated azomethine N-oxides 1 with substituted N-arylmaleimides 2 leads to the synthesis of new stereoisomeric 2,5-diaryl-3-(o-nitro)-styryl-4H-2,3,3a,5,6,6a-hexahydropyrrolo [3,4-d] isoxazole-4,6-dione derivatives 3 in excellent yield. These stereoisomers have been characterized as cis-3A and trans-3B on the basis of their spectral measurements and are obtained in the ratio of almost 1:2 respectively in all the reaction, which is the reverse of the stereoisomers obtained through the 'Huisgen reaction’ of C,N-diaryl nitrones with N-aryl maleimides as reported earlier from these laboratories. | 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(03) [March 1999] | en_US |
| dc.title | 1,3-Dipolar cycloaddition reactions of substituted open-chain conjugated azomethine N-oxides with substituted N-arylmaleimides leading to the synthesis of new stereoisomeric 2,5 -diaryl-3- (o-nitro)-styryl -4H-2,3,3a,5,6,6a- hexahydropyrrolo [3,4-d] isoxazole-4, 6-dione derivatives | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(03) [March 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(3) 292-296.pdf | 972.62 kB | Adobe PDF | View/Open |
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