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首页> 外文期刊>Angewandte Chemie >Nickel-Catalyzed Cross-Coupling of Sulfonamides With (Hetero)aryl Chlorides
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Nickel-Catalyzed Cross-Coupling of Sulfonamides With (Hetero)aryl Chlorides

机译:用(杂)芳基氯化物镍催化的磺酰胺交联偶联

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摘要

The development of Ni-catalyzed C-N cross-couplings of sulfonamides with (hetero)aryl chlorides is reported. These transformations, which were previously achievable only with Pd catalysis, are enabled by use of air-stable (L)NiCl(o-tol) pre-catalysts (L=PhPAd-DalPhos and PAd2-DalPhos), without photocatalysis. The collective scope of (pseudo)halide electrophiles (X=Cl, Br, I, OTs, and OC(O)NEt2) demonstrated herein is unprecedented for any reported catalyst system for sulfonamide C-N cross-coupling (Pd, Cu, Ni, or other). Preliminary competition experiments and relevant coordination chemistry studies are also presented.
机译:报道了Ni催化的磺胺酰胺与(杂)芳基氯化物的C-N交叉偶联。 通过使用空气稳定(L)NiCl(O-Tol)预催化剂(L = PhPad-Dalphos和Pad2-Dalphos),这些转化仅通过PD催化来实现,所述转化仅通过使用空气稳定(L)NiCl(o-Tol)预催化剂(L = PhPad-Dalphos和PAD2-Dalphos)而无需光催化。 本文所证明的(伪)卤化物电泳(X = Cl,Br,I,OTS和OC(O)NET2)的集体范围对于磺酰胺CN交叉偶联(Pd,Cu,Ni或 其他)。 还提出了初步竞争实验和相关协调化学研究。

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