Mechanistic Insights into the Base-Mediated Deuteration of Pyridyl Phosphonium and Ammonium Salts

08 October 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Pyridines can be deuterated at remote sites by treatment with KOtBu in DMSO-d6, although without discrimination between the meta- and para-position. Herein, base-catalyzed deuterations have been studied, computationally and experimentally, on a series of pyridyl phosphonium and ammonium salts having a temporary electron-withdrawing group to block the para-position while increasing the acidity in the other positions.

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