Abstract
An electrochemical initiated tandem reaction of anilines with 2-formyl benzonitrile has been developed. Thus, unprecedented 3-N-aryl substituted isoindolinones have been conveniently achieved by constant current electrolysis in a divided cell using catalytic amount of electricity and supporting electrolyte and a Pt-cathode as working electrode. The origin of the electrochemical activation as well as the mechanism of the subsequent chemical cascade reactions have been investigated by DFT calculations.
Subject
Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science
Reference30 articles.
1. Kerru, N., Gummidi, L., Maddila, S., Gangu, K.K., and Jonnalagadda, S.B. (2020). A Review on Recent Advances in Nitrogen-Containing Molecules and Their Biological Applications. Molecules, 9.
2. Isoindolinone-based inhibitors of the MDM2-p53 protein-protein interaction;Bioorg. Med. Chem. Lett.,2005
3. Analysis of Chemical Shift Changes Reveals the Binding Modes of Isoindolinone Inhibitors of the MDM2-p53 Interaction;J. Am. Chem. Soc.,2008
4. Schubert, G., Rieke-Zapp, J., Keil, J., Kleemann, H.W., Hanna, R., Huang, B.G., Wu, X.D., and Gouraud, Y. (2005). Process for Preparing (3-Oxo-2,3-dihydro-1H-isoindol-1-yl) Acetylguanidine Derivatives. (US20050124681), U.S. Patent.
5. Isoindolin-1-one derivatives as urease inhibitors: Design, synthesis, biological evaluation, molecular docking and in-silico ADME evaluation;Bioorg. Chem.,2019
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