Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/455
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dc.contributor.authorDubey, P K-
dc.contributor.authorReddy, P V V Prasada-
dc.contributor.authorSrinivas, K-
dc.date.accessioned2008-03-24T06:26:53Z-
dc.date.available2008-03-24T06:26:53Z-
dc.date.issued2007-03-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/455-
dc.description488-491en_US
dc.description.abstract2-(⍺-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.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl⁸ C07Den_US
dc.sourceIJCB Vol.46B(3) [March 2007]en_US
dc.subject1-Substituted-2-(⍺–chloroalkyl)benzimidazoleen_US
dc.subjectAr-SO₂- Na⁺en_US
dc.subjectTEBACen_US
dc.subjectSulphonesen_US
dc.titleSynthesis of 1-alkyl/aralkyl-2- (1-arylsulfonylalkyl) benzimidazoles under PTC conditionsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(03) [March 2007]

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