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IJC-B Vol.44B [2005] >
IJC-B Vol.44B(06) [June 2005] >

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
IPC CodeInt.Cl.7 C 07 D 233/54
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 acetyla¬≠tion 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.
Page(s): 1298-1300
ISSN: 0975-0983(Online); 0376-4699(Print)
Source:IJC-B Vol.44B(06) [June 2005]

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