Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9123
Title: Synthesis and reactions of 4-(aminoaryl)-methylene-2-aryl-2-imidazolin-5-ones
Authors: Shafi, P M
Sobha, T D
Basheer, P A M
Waibel, R
Issue Date: Jun-2005
Publisher: CSIR
Series/Report no.: <b>Int</b>.<b>Cl</b>.<b><sup>7</sup> C 07 D 233/54</b>
Abstract: Benzimidic 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 <sup>13</sup>C assignment of some of the carbon atoms of one of the acetyl derivatives has been done by HMQC and HMBC experiments.
Description: 1298-1300
URI: http://hdl.handle.net/123456789/9123
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(06) [June 2005]

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