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http://nopr.niscpr.res.in/handle/123456789/6775Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kotha, Sambasivarao | - |
| dc.contributor.author | Behera, Manoranjan | - |
| dc.date.accessioned | 2009-12-09T10:47:07Z | - |
| dc.date.available | 2009-12-09T10:47:07Z | - |
| dc.date.issued | 2006-12 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/6775 | - |
| dc.description | 2684-2689 | en_US |
| dc.description.abstract | A general methodology for the synthesis of various symmetrical and unsymmetrical tetraphenylmethane (TPM) derivatives is reported using the Suzuki-Miyaura (SM) cross-coupling reaction as a key step. The formation of an interesting self-coupling product 14 during the SM cross-coupling reaction of mono-iodo tetraphenylmethane derivative 5 is also observed. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl.8 C07C | en_US |
| dc.source | IJC-B Vol.45B(12) December 2006] | en_US |
| dc.subject | Suzuki-Miyaura coupling | en_US |
| dc.subject | carbon-rich compounds | en_US |
| dc.subject | palladium | en_US |
| dc.subject | nanostructures | en_US |
| dc.subject | boron | en_US |
| dc.subject | tetraphenylmethane | en_US |
| dc.title | Preparation of functionalised tetraphenylmethane derivatives via the Suzuki-Miyaura cross-coupling reaction | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.45B(12) December 2006] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 45B(12) 2684-2689.pdf | 121.82 kB | Adobe PDF | View/Open |
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