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"One-pot" synthesis of amidoxime via Pd-catalyzed cyanation and amidoximation.

Journal Article


Abstract


  • A novel "one-pot" reaction was developed for the synthesis of aryl or heteroaryl-substituted amidoxime compounds containing various functional groups. Fluorescence titration experiments coupled with theoretical analysis revealed that the steric hindrance and electronic effects of substituents influence the binding ability of the amidoxime compounds to uranyl ions.

Publication Date


  • 2015

Citation


  • Yang, C. -T., Han, J., Liu, J., Gu, M., Li, Y., Wen, J., . . . Wang, X. (2015). "One-pot" synthesis of amidoxime via Pd-catalyzed cyanation and amidoximation.. Organic & biomolecular chemistry, 13(9), 2541-2545. doi:10.1039/c4ob02456g

Web Of Science Accession Number


Start Page


  • 2541

End Page


  • 2545

Volume


  • 13

Issue


  • 9

Abstract


  • A novel "one-pot" reaction was developed for the synthesis of aryl or heteroaryl-substituted amidoxime compounds containing various functional groups. Fluorescence titration experiments coupled with theoretical analysis revealed that the steric hindrance and electronic effects of substituents influence the binding ability of the amidoxime compounds to uranyl ions.

Publication Date


  • 2015

Citation


  • Yang, C. -T., Han, J., Liu, J., Gu, M., Li, Y., Wen, J., . . . Wang, X. (2015). "One-pot" synthesis of amidoxime via Pd-catalyzed cyanation and amidoximation.. Organic & biomolecular chemistry, 13(9), 2541-2545. doi:10.1039/c4ob02456g

Web Of Science Accession Number


Start Page


  • 2541

End Page


  • 2545

Volume


  • 13

Issue


  • 9