CYCLOADDITION APPROACH FOR THE SYNTHESIS OF SOME HINDERED N-BENZOYLIMIDAZOLES

Authors
RAJAKUMAR P KANNAN A SUJATHA R
Citation
P. Rajakumar et al., CYCLOADDITION APPROACH FOR THE SYNTHESIS OF SOME HINDERED N-BENZOYLIMIDAZOLES, Synthetic communications, 24(13), 1994, pp. 1847-1853
Citations number
3
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthetic communications → ACNP
ISSN journal
00397911
Volume
24
Issue
13
Year of publication
1994
Pages
1847 - 1853
Database
ISI
SICI code
0039-7911(1994)24:13<1847:CAFTSO>2.0.ZU;2-Q
Abstract
Cycloaddition of N-Benzoyl-4,5-diphenyl-2-strylimidazole to 2,5-dimeth yl-3,4-diphenylcyclopentadienone, tetraphenylcyclopentadienone, 1,3-di phenylisobenzofuran and tetraphenylcyclopentadiene afforded the substi tuted and hindered imidazoles 2a,2b,2c & 2d. The N-benzoyl styrylimida zole 4 derived from phenanthrenequinone, cinnamaldehyde and ammonium a cetate also underwent similar cycloaddition.