An efficient route towards the synthesis of monosubstituted N-aryl amidines from 4,5-Dihydro-1,2,4-oxadiazoles

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Abstract

4,5-Dihydro-1,2,4-oxadiazoles were prepared using 1,3-dipolar cycloaddition of imines with nitrile oxides. Further reductive N-O bond cleavage furnished monosubstituted N-aryl amidines in good yield. Thus an efficient route for the synthesis of monosubstituted N-aryl amidines has been developed.

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Chavan, N. L., Naik, N. H., Nayak, S. K., & Kusurkar, R. S. (2010). An efficient route towards the synthesis of monosubstituted N-aryl amidines from 4,5-Dihydro-1,2,4-oxadiazoles. Arkivoc, 2010(2), 248–255. https://doi.org/10.3998/ark.5550190.0011.220

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