首页> 外文期刊>Organic letters >Two-Step, One-Pot Ni-Catalyzed Neopentylglycolborylation and Complementary Pd/Ni-Catalyzed Cross-Coupling with Aryl Halides, Mesylates, and Tosylates
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Two-Step, One-Pot Ni-Catalyzed Neopentylglycolborylation and Complementary Pd/Ni-Catalyzed Cross-Coupling with Aryl Halides, Mesylates, and Tosylates

机译:两步一锅镍催化的新戊基糖基化和互补的钯/镍催化的交叉偶联,包括芳基卤化物,甲磺酸盐和甲苯磺酸盐

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摘要

Two-step, one-pot neopentylglycolborylation of aryl iodides and bromides catalyzed by NiCl2(dppe) and NiCl2(dppp) is reported. Electron-rich and electron-deficient aryl neopentylglycolboronates were efficiently cross-coupled with aryl iodides, bromides, chlorides, mesylates, and tosylates by exploiting complementary Pd/Ni and Ni/Ni catalysis. The borylation route was further extended to a three-step, one-pot synthesis of biaryls via in situ Ni-catalyzed borylation and Pd-mediated cross-coupling.
机译:据报道,NiCl2(dppe)和NiCl2(dppp)催化芳基碘和溴化物的两步一锅新戊基乙二醇化反应。通过利用互补的Pd / Ni和Ni / Ni催化作用,富电子和缺电子的芳基新戊基乙二醇硼酸酯可以有效地与芳基碘化物,溴化物,氯化物,甲磺酸盐和甲苯磺酸盐交叉偶联。硼化途径通过原位镍催化的硼化和Pd介导的交叉偶联进一步扩展为三步一锅合成联芳基。

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