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http://nopr.niscpr.res.in/handle/123456789/58674Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sathya, V | - |
| dc.contributor.author | Venkatesan, N | - |
| dc.contributor.author | Heera, T R | - |
| dc.contributor.author | Sivakumar, M N | - |
| dc.date.accessioned | 2021-12-24T04:53:43Z | - |
| dc.date.available | 2021-12-24T04:53:43Z | - |
| dc.date.issued | 2021-09 | - |
| dc.identifier.issn | 0975-0991 (Online); 0971-457X (Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/58674 | - |
| dc.description | 649-652 | en_US |
| dc.description.abstract | Synthesis of indole based novel symmetrical nitroolefinic dendritic core has been succeeded using N-arylation route followed by Henry reaction. Synthesized symmetrical 1,3,5-triindolyl benzene has been successfully synthesis of by N-arylation of indole, symmetrical 1,3,5-tri(3-formyl indolyl)benzene and 1,3,5-tris(3-((E)-2-nitrovinyl)-1H-indol-1yl)benzene followed by Hendry reaction. These nitroolefinic cores have potential application in theoretical and medicinal chemistry and also used to prepare many new organic compounds of indole derivatives. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | NIScPR-CSIR, India | en_US |
| dc.source | IJCT Vol.28(5) [September 2021] | en_US |
| dc.subject | Dendritic core | en_US |
| dc.subject | Henry reaction | en_US |
| dc.subject | Indole | en_US |
| dc.subject | N-arylation | en_US |
| dc.subject | Nitroolefin | en_US |
| dc.title | Synthesis of indole based novel symmetrical nitroolefinic dendritic core through n-arylation route | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJCT Vol.28(5) [September 2021] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCT 28(5) 649-652.pdf | 553.01 kB | Adobe PDF | View/Open |
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