Please use this identifier to cite or link to this item:
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.: Int.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 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.
Description: 1298-1300
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(06) [June 2005]

Files in This Item:
File Description SizeFormat 
IJCB 44B(6) 1298-1300.pdf39.81 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.