Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/9123
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dc.contributor.authorShafi, P M-
dc.contributor.authorSobha, T D-
dc.contributor.authorBasheer, P A M-
dc.contributor.authorWaibel, R-
dc.date.accessioned2010-05-31T09:57:07Z-
dc.date.available2010-05-31T09:57:07Z-
dc.date.issued2005-06-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9123-
dc.description1298-1300en_US
dc.description.abstractBenzimidic acid methyl esters on heating with glycine ester in toluene in presence of sodium acetate yield 4-(aminoaryl)­methylene-2-aryl-2-imidazolin-5-ones. They undergo acetyla­tion and benzoylation on reaction with acetic anhydride and benzoyl chloride, respectively. The 13C assignment of some of the carbon atoms of one of the acetyl derivatives has been done by HMQC and HMBC experiments.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 233/54en_US
dc.sourceIJC-B Vol.44B(06) [June 2005]en_US
dc.titleSynthesis and reactions of 4-(aminoaryl)-methylene-2-aryl-2-imidazolin-5-onesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(06) [June 2005]

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