Litcius/Paper detail

C3 Selective Hydroxylation of Pyridines via Photochemical Valence Isomerization of Pyridine <i>N</i>-Oxides

Chen‐Yan Cai, Si-Jie Chen, Rohan R. Merchant, Yuzuru Kanda, Tian Qin

2024Journal of the American Chemical Society37 citationsDOIOpen Access PDF

Abstract

The C–H hydroxylation of the pyridine C3 position is a highly desirable transformation but remains a great challenge due to the inherent electronic properties of this heterocycle core which bring difficulties in chemical reactivity and regioselectivity. Herein we present an efficient method for formal C3 selective hydroxylation of pyridines via photochemical valence isomerization of pyridine N -oxides. This metal-free transformation features operational simplicity and compatibility with a diverse array of functional groups, and the resulting hydroxylated products are amenable to further elaboration to synthetically useful building blocks. The synthetic utility of this strategy is further demonstrated in the effective late-stage functionalization of pyridine-containing medicinally relevant molecules and versatile derivatizations of 3-pyridinols.

Topics & Concepts

ChemistryHydroxylationPyridineIsomerizationRegioselectivityValence (chemistry)Combinatorial chemistryMoleculePhotochemistryOrganic chemistryCatalysisEnzymeCatalytic C–H Functionalization MethodsRadical Photochemical ReactionsOxidative Organic Chemistry Reactions
C3 Selective Hydroxylation of Pyridines via Photochemical Valence Isomerization of Pyridine <i>N</i>-Oxides | Litcius