Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/24777
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dc.contributor.authorYadav, Tej Bahadur-
dc.contributor.authorSingh, Virendra-
dc.date.accessioned2013-12-13T11:52:15Z-
dc.date.available2013-12-13T11:52:15Z-
dc.date.issued2013-12-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/24777-
dc.description1536-1539en_US
dc.description.abstractA novel one-pot ecofriendly synthesis of 2,5,6-trisubstituted-1H-benzimidazole nucleoside derivatives have been accomplished stepwise. i.e. substituted o-phenylenediamine and aldoses using iodine as an oxidant or promoter in acetic solution at room temperature. A practical method has been developed for conversion of unprotected and unmodified aldoses to aldo-benzimidazoles.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.52B(12) December 2013]en_US
dc.subjectBenzimidazoleen_US
dc.subjectNucleosidesen_US
dc.subjecto-phenylenediamineen_US
dc.subjectIodineen_US
dc.subjectAcetic aciden_US
dc.subjectAldosesen_US
dc.titleIodine promoted simple synthesis of benzimidazole acyclonucleosidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.52B(12) December 2013]

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