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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 24, 1994 - Issue 13
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Original Articles

Cycloaddition Approach for the Synthesis of Some Hindered N-Benzoylimidazoles

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Pages 1847-1853 | Received 13 Dec 1993, Published online: 23 Sep 2006
 

Abstract

Cycloaddition of N-Benzoyl-4,5-diphenyl-2-strylimidazole to 2,5-dimethyl-3,4-diphenylcyclopentadienone, tetraphenylcyclopentadienone, 1,3-diphenylisobenzofuran and tetraphenylcyclopentadiene afforded the substituted and hindered imidazoles 2a,2b,2c & 2d. The N-benzoyl styrylimidazole 4 derived from phenanthrenequinone, cinnamaldehyde and ammonium acetate also underwent similar cycloaddition.

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