計算化学を駆使してケトンの新規光触媒機能を発見〜カルボン酸の新たな分子変換技術が医薬品探索研究を推進〜

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2025-07-07 静岡県立大学,北海道大学

静岡県立大学と北海道大学連携グループは、ケトン(キサントン)が光照射下で安価かつ金属不要にカルボキシラジカルを生成する新しい光触媒機能を、計算化学と実験で発見しました。これにより、脂肪族カルボン酸の脱炭酸的官能基化や芳香族カルボン酸の位置選択的C–Hアルキル化が可能に。これら反応は医薬品探索に有効で、持続可能・環境調和的な合成への応用が期待されます。論文はJACS誌に掲載。

計算化学を駆使してケトンの新規光触媒機能を発見〜カルボン酸の新たな分子変換技術が医薬品探索研究を推進〜
図1.ケトンの新規光触媒作用:カルボキシラジカルの選択的調製

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光活性化されたケトン触媒によるカルボキシラジカルの直接的生成 Direct Generation of Carboxyl Radicals from Carboxylic Acids Catalyzed by Photoactivated Ketones

Kenji Yamashita,Hayate Sano,Yuki Goto,Hiroki Hayashi,and Yoshitaka Hamashima
Journal of the American Chemical Society  Published: July 2, 2025
DOI:https://doi.org/10.1021/jacs.5c04571

Abstract

Carboxyl radicals are reactive intermediates, which potentially offer opportunities to develop unique transformations in radical chemistry, yet their straightforward generation from carboxylic acids has largely relied on the use of environmentally less benign methods, and their application has been mainly limited to decarboxylative functionalizations. Here, we present a photoactivated ketone-catalyzed direct generation of carboxyl radicals via hydrogen atom transfer (HAT) from the O–H bond of carboxylic acids. An integrated approach combining theoretical predictions and experimental validation guided the development of this simple, chemoselective O–H HAT catalysis, which is facilitated by hydrogen-bonding interaction between the ketone photocatalyst and the carboxylic acid and leaves weaker C–H bonds intact. Our protocol has a broad substrate scope with high functional group tolerance and is applicable to direct decarboxylative functionalization of primary, secondary, and tertiary aliphatic carboxylic acids, including bioactive molecules. Benzoyloxy radicals were also prepared, enabling site-selective C(sp3)–H alkylation of ortho-alkyl-substituted benzoic acids via a 1,5-HAT process.

有機化学・薬学
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