Abstract
The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organic
synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds
to truncating retrosynthetic plans, there is a growing need for new reagents and methods for
achieving such a transformation in both academic and industrial circles. One main drawback of
current chemical reagents is the lack of diversity with regards to structure and reactivity that
prevent a combinatorial approach for rapid screening to be employed. In that regard, directed
evolution still holds the greatest promise for achieving complex C–H oxidations in a variety of
complex settings. Herein we present a rationally designed platform that provides a step towards
this challenge using N-ammonium ylides as electrochemically driven oxidants for site-specific,
chemoselective C(sp3)–H oxidation. By taking a first-principles approach guided by computation,
these new mediators were identified and rapidly expanded into a library using ubiquitous building
blocks and trivial synthesis techniques. The ylide-based approach to C–H oxidation exhibits
tunable selectivity that is often exclusive to this class of oxidants and can be applied to real world
problems in the agricultural and pharmaceutical sectors.