C-H Functionalization of Pyridines via Oxazino Pyridine Intermediates: Switching to -Selectivity under Acidic Conditions.

-Selective C-H functionalization of pyridines holds a significant value but remains underdeveloped. Site-switchable C-H functionalization of pyridines under easily tunable conditions expedites drug development. We recently reported a redox-neutral dearomatization-rearomatization strategy for -C-H functionalization of pyridines via oxazino pyridine intermediates. Here, we demonstrate that these oxazino pyridine intermediates undergo highly -selective functionalization simply by switching to acidic conditions. A broad scope of -alkylated and arylated pyridines is prepared through radical as well as ionic pathways. These mild and catalyst-free methods are applied to the late-stage -functionalization of drugs using pyridines as the limiting reagents. Consecutive -difunctionalization of pyridines is also achieved with complete regiocontrol relying on the pH-dependent reactivity of oxazino pyridines.