C–C Bond Cleavage at the N-α Position Enabled by the Low-potential Electrochemical Oxidation of the 2,7-Dimethoxynaphthyl Electroauxiliary

1Citations
Citations of this article
N/AReaders
Mendeley users who have this article in their library.

Abstract

Herein, we report that the 2,7-dimethoxynaphthyl (2,7-DMN) group is a novel electroauxiliary that is readily installed at the N-α position of a carbamate through Friedel–Crafts-type arylation. The resulting N-α C–C bond is easily cleaved through low-potential electrochemical oxidation to give the corresponding iminium cation.

Cite

CITATION STYLE

APA

Okamoto, K., Imada, Y., Shida, N., Kitano, Y., Atobe, M., & Chiba, K. (2023). C–C Bond Cleavage at the N-α Position Enabled by the Low-potential Electrochemical Oxidation of the 2,7-Dimethoxynaphthyl Electroauxiliary. Electrochemistry, 91(11). https://doi.org/10.5796/electrochemistry.23-67076

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free