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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Dubey, P K | - |
| dc.contributor.author | Reddy, P V V Prasada | - |
| dc.contributor.author | Srinivas, K | - |
| dc.date.accessioned | 2008-03-24T06:26:53Z | - |
| dc.date.available | 2008-03-24T06:26:53Z | - |
| dc.date.issued | 2007-03 | - |
| dc.identifier.issn | 0376-4699 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/455 | - |
| dc.description | 488-491 | en_US |
| dc.description.abstract | 2-(⍺-chloroalkyl)benzimidazoles 1 on reaction with arylsulphinate sodium salt 2, in CH₃CN under PTC conditions, gives 3 which on alkylation yields 1-alky/aralkyl-2-(⍺-aryl sulfonylalkyl) benzimidazoles 4. Alternatively, 4 can also be prepared by the reaction of 2 with 1-alkyl/aralkyl-2- (⍺–chloroalkyl) benzimidazole 5 in CH₃CN using triethylbenzylammonium chloride (TEBAC) as PTC. 5 are obtained from 1 in turn, by alkylation in CH₃CN under PTC conditions. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl⁸ C07D | en_US |
| dc.source | IJCB Vol.46B(3) [March 2007] | en_US |
| dc.subject | 1-Substituted-2-(⍺–chloroalkyl)benzimidazole | en_US |
| dc.subject | Ar-SO₂- Na⁺ | en_US |
| dc.subject | TEBAC | en_US |
| dc.subject | Sulphones | en_US |
| dc.title | Synthesis of 1-alkyl/aralkyl-2- (1-arylsulfonylalkyl) benzimidazoles under PTC conditions | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.46B(03) [March 2007] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 46B(3) (2007) 488-491.pdf | 106.53 kB | Adobe PDF | View/Open |
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