| Literature DB >> 31483627 |
Philip L Norcott1, Chelsey L Hammill1, Benjamin B Noble1, Johnathon C Robertson2, Angus Olding2, Alex C Bissember2, Michelle L Coote1.
Abstract
Bench- and air-stable 1-methoxy-2,2,6,6-tetramethylpiperidine (TEMPO-Me) is relatively unreactive at ambient temperature in the absence of an electrochemical stimulus. In this report, we demonstrate that the one-electron electrochemical oxidation of TEMPO-Me produces a powerful electrophilic methylating agent in situ. Our computational and experimental studies are consistent with methylation proceeding via a SN2 mechanism, with a strength comparable to the trimethyloxonium cation. A protocol is developed for the electrochemical methylation of aromatic acids using TEMPO-Me.Entities:
Year: 2019 PMID: 31483627 DOI: 10.1021/jacs.9b08634
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419