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Despite their value, direct access from their aromatic precursors under Birch conditions remains limited due to safety, as well as chemoselectivity challenges. In this context, energy\u2010transfer (EnT)\u2010enabled Birch\u2010type reductions have emerged as a powerful strategy for (chemo)selective product formation. However, it has been largely confined to bicyclic (hetero)arenes, while their more prevalent monocyclic counterparts remain vastly underexplored. Herein, we describe the triplet sensitized, partial saturation of 2\u2010pyridones and their derivatives, which are known as privileged scaffolds in drug discovery. Our methodology shows exceptional regioselectivity for the Birch\u2010type product and tolerates a vast number of functional groups, bypassing conventional highly reducing reaction conditions. 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