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Williams, Oliver P.; Chmiel, Alyah F.; Mikhael, Myriam; Bates, Desiree M.; Yeung, Charles S.; Wickens, Zachary K.
Angewandte Chemie, April 24, 2023, Letnik: 62, Številka: 18Journal Article
Herein, we describe a practical protocol for the removal of alcohol functional groups through reductive cleavage of their benzoate ester analogs. This transformation requires a strong single electron transfer (SET) reductant and a means to accelerate slow fragmentation following substrate reduction. To accomplish this, we developed a photocatalytic system that generates a potent reductant from formate salts alongside Brønsted or Lewis acids that promote fragmentation of the reduced intermediate. This deoxygenation procedure is effective across structurally and electronically diverse alcohols and enables a variety of difficult net transformations. This protocol requires no precautions to exclude air or moisture and remains efficient on multigram scale. Finally, the system can be adapted to a one‐pot benzoylation‐deoxygenation sequence to enable direct alcohol deletion. Mechanistic studies validate that the role of acidic additives is to promote the key C(sp3)−O bond fragmentation step. A new protocol for alcohol deoxygenation that functions across a wide range of alcohol structures is reported. This approach combines the reductive potency of carbon dioxide radical anion with acidic additives to promote the kinetically slow C(sp3)−O bond cleavage.
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in: SICRIS
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