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Photoredox-catalyzed selective deuterodefluorination of α,α-difluoroarylacetic esters and amides
Organic Chemistry Frontiers ( IF 4.6 ) Pub Date : 2024-06-22 , DOI: 10.1039/d4qo00781f
Zi-Hang Yuan 1 , Hong Xin 1 , Yuan Gao 1 , Guo-Wei Sun 1 , Rui-Ying Zhao 1 , Xin-Hua Duan 1, 2 , Li-Na Guo 1
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A highly selective photocatalytic deuterodefluorination of fluorinated esters with D2O is presented. By tailoring the catalytic system, a variety of α,α-difluoroaryl acetates underwent selective defluorination/deuteration to afford the 2-fluoro-2-arylacetate-d and 2-arylacetate-d2 in good yields with excellent deuteration rate. Satisfactorily, this protocol was successfully applied to deuterate some drug molecules, such as the felbinacethyl-d2 and felbilnac-d2.

中文翻译:


光氧化还原催化α,α-二氟芳基乙酸酯和酰胺的选择性氘代脱氟



提出了一种用 D 2 O 氟化酯的高选择性光催化氘代脱氟反应。通过定制催化体系,多种α,α-二氟芳基乙酸酯进行选择性脱氟/氘化,以良好的产率和优异的产率得到2-氟-2-芳基乙酸酯-d和2-芳基乙酸酯-d 2 氘化速率。令人满意的是,该方案成功应用于氘化一些药物分子,例如 felbinacethyl-d 2 和 felbilnac-d 2
更新日期:2024-06-26
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