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http://nopr.niscpr.res.in/handle/123456789/6791Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jing, Xiaobi | - |
| dc.contributor.author | Xu, Feng | - |
| dc.contributor.author | Zhu, Qihua | - |
| dc.contributor.author | Ren, Xinfeng | - |
| dc.contributor.author | Li, Dong | - |
| dc.contributor.author | Yan, Chaoguo | - |
| dc.contributor.author | Shi, Yaocheng | - |
| dc.date.accessioned | 2009-12-09T11:08:46Z | - |
| dc.date.available | 2009-12-09T11:08:46Z | - |
| dc.date.issued | 2006-12 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/6791 | - |
| dc.description | 2781-2783 | en_US |
| dc.description.abstract | Adsorbed on clayfen together with p-toluenesulfonic acid and catalytic amount of tin tetrachloride anhydrous (5%), aryl ketones are readily turned to 1,3,5-triarylbenzenes in good yields upon exposure to microwaves under solvent-free conditions. A new method for the synthesis of poly substituted benzene is developed, which is simple and rapid. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl.8 C07D | en_US |
| dc.source | IJC-B Vol.45B(12) December 2006] | en_US |
| dc.subject | 1,3,5-triarylbenzenes | en_US |
| dc.subject | p-toluenesulfonic acid | en_US |
| dc.subject | tin tetrachloride anhydrous | en_US |
| dc.subject | clayfen | en_US |
| dc.title | New method for the synthesis of 1,3,5-triarylbenzenes | 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) 2781-2783.pdf | 162.32 kB | Adobe PDF | View/Open |
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