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dc.contributor.authorKidwai, Mazaahir-
dc.contributor.authorPriya-
dc.date.accessioned2009-01-13T05:46:16Z-
dc.date.available2009-01-13T05:46:16Z-
dc.date.issued2008-12-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/2751-
dc.description1876-1881en_US
dc.description.abstractAn environmentally benign approach for the synthesis of 2-aryl-3H-quinazolin-4-ones employing sodium perborate (SPB) as catalyst is described. SPB in water and acetone system is proved as selective catalyst of hydration for cyanides. The rate enhancement and high yield is attributed to the coupling of suitable catalyst with the solvent system. The key step is the microwave prompted reaction sequence combining 2-aminobenzonitrile and aromatic/heteroaromatic aldehydes providing efficient access to intermediate for the synthesis of this important class of nitrogen fused heterocycle.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(12) [December 2008]en_US
dc.subjectSodium perborateen_US
dc.subjectQuinazolin-4-onesen_US
dc.subject2-aminobenzonitrileen_US
dc.subjectMicrowave irradiation (MWI)en_US
dc.subjectSolvent-systemen_US
dc.titleSynthesis of quinazolinone analogues using sodium perborate as catalysten_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(12) December 2008]

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