- A new route for the convenient synthesis of imidazo[2,1-b]-1,3,4-oxadiazoles and their fungitoxicity
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5-Aryl-1-arylideneamino-1,3,4-oxadiazoles (4a-f) react with trichloroacetic acid with the evolution of carbon dioxide to furnish 5-aryl-2-[(1-aryl-2,2,2-trichloroethyl)amino]-1,3,4-oxadiazoles (6a-f), which undergo ring closure with primary arylamines to
- Yadav,Saigal, Sandhya,Shukla, Supriya
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p. 385 - 387
(2007/10/03)
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