Hypervalent iodine oxidation of 1-phenyl-3-arylpyrazole-4-carboxaldehyde oximes: A facile and efficient synthesis of new 3,4-bis(1-phenyl-3- arylpyrazolyl)-1,2,5-oxadiazole-N-oxides

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Abstract

Oxidation of pyrazole-4-carboxaldehyde oximes 2 with iodobenzene diacetate leads to dimerization of initially formed nitrile oxides, thereby offering an easy and efficient method for the synthesis of new 3,4-bis(1-phenyl-3- arylpyrazolyl)-1,2,5-oxadiazole-N-oxides (4). © ARKAT USA, Inc.

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Prakash, O., & Pannu, K. (2007). Hypervalent iodine oxidation of 1-phenyl-3-arylpyrazole-4-carboxaldehyde oximes: A facile and efficient synthesis of new 3,4-bis(1-phenyl-3- arylpyrazolyl)-1,2,5-oxadiazole-N-oxides. Arkivoc, 2007(13), 28–33. https://doi.org/10.3998/ark.5550190.0008.d04

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