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首页> 外文期刊>Chemistry - A European Journal >Palladium-Catalyzed Borylation of Aryl Mesylates and Tosylates and Their Applications in One-Pot Sequential Suzuki–Miyaura Biaryl Synthesis
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Palladium-Catalyzed Borylation of Aryl Mesylates and Tosylates and Their Applications in One-Pot Sequential Suzuki–Miyaura Biaryl Synthesis

机译:钯催化的甲磺酸烷基酯和甲苯磺酸酯的硼化反应及其在一锅顺序铃木-宫浦联芳的合成中的应用

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Top of the one-pots! The first palladium-catalyzed borylation of aryl tosylates and mesylates is described. The reaction conditions are mild and provide excellent functional-group compatibility (e.g., R=CN, CHO, COOMe, C(O)R, NH2, or NH-indole; see scheme). Pd/MeO-CM-phos allows one-pot sequential reactions in the preparation of unsymmetrical biaryls.
机译:一锅之巅!描述了芳基甲苯磺酸酯和甲磺酸酯的第一钯催化的硼化。反应条件温和并且提供优异的官能团相容性(例如,R = CN,CHO,COOMe,C(O)R,NH 2 或NH-吲哚;参见方案)。 Pd / MeO-CM-phos可以在不对称联芳基的制备中进行一锅法连续反应。

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