Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6780
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dc.contributor.authorPasha, M A-
dc.contributor.authorJayashankara, V P-
dc.date.accessioned2009-12-09T11:06:02Z-
dc.date.available2009-12-09T11:06:02Z-
dc.date.issued2006-12-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6780-
dc.description2716-2719en_US
dc.description.abstract2,3-Dihydro-1H-1,5-benzodiazepines have been synthesized by the condensation of o-phenylenediamine and cyclic or acyclic ketones in the presence of CdCl2 as catalyst at 80-85ºC temperature. The yields are high and the reactions go to completion within 10-20 min. en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.8 C07Den_US
dc.sourceIJC-B Vol.45B(12) December 2006]en_US
dc.subject2,3-Dihydro-1H-1,5-benzodiazepinesen_US
dc.subjecto-phenylenediamineen_US
dc.subjectketonesen_US
dc.subjectCdCl2en_US
dc.subjectsolvent-free reactionen_US
dc.titleAn expeditious synthesis of 1,5-benzodiazepine derivatives catalyzed by CdCl2en_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(12) December 2006]

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