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首页> 外文期刊>Organic letters >Palladium-Catalyzed Arylation of α-Methylene-γ-butyrolactone: 3-Benzylfuran-2(5H)-ones vs (Z)-Benzylidene-γ-butyrolactones and Their Reduction to 3-Benzyl-γ-butyrolactones
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Palladium-Catalyzed Arylation of α-Methylene-γ-butyrolactone: 3-Benzylfuran-2(5H)-ones vs (Z)-Benzylidene-γ-butyrolactones and Their Reduction to 3-Benzyl-γ-butyrolactones

机译:钯催化的α-亚甲基-γ-丁内酯的芳基化:3-苄基呋喃-2(5H)-对vs(Z)-苄基-γ-丁内酯及其还原为3-苄基-γ-丁内酯

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摘要

The palladium-catalyzed arylation of the α-methylene-γ-butyrolactone proceeds in good yields and may be directed toward the synthesis of 3-benzylfuran-2(5H)-ones when the starting aryl iodides contain strongly electron-withdrawing groups. The combined palladium-catalyzed arylation/hydrogenation of the α-methylene-γ-butyrolactone represents a new simple entry into functionalized α-benzyl-γ-butyrolactones.
机译:钯催化的α-亚甲基-γ-丁内酯的芳基化反应收率很高,当起始芳基碘化物含有强吸电子基团时,可直接用于3-苄基呋喃-2(5H)-的合成。钯催化的α-亚甲基-γ-丁内酯的芳基化/加氢反应代表了功能性α-苄基-γ-丁内酯的新的简单进入。

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