共 80 条
Mechanism and Selectivity in Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Halides with Alkyl Halides
被引:533
作者:

Biswas, Soumik
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h-index: 0
机构:
Univ Rochester, Dept Chem, Rochester, NY 14627 USA Univ Rochester, Dept Chem, Rochester, NY 14627 USA

Weix, Daniel J.
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h-index: 0
机构:
Univ Rochester, Dept Chem, Rochester, NY 14627 USA Univ Rochester, Dept Chem, Rochester, NY 14627 USA
机构:
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
关键词:
FUNCTIONALIZED GRIGNARD-REAGENTS;
REDUCTIVE CONJUGATE ADDITION;
CARBON BOND FORMATION;
OXIDATIVE ADDITION;
RADICAL CATALYSIS;
ORGANIC HALIDES;
AROMATIC HALIDES;
KETONE FORMATION;
DIRECT ARYLATION;
COMPLEXES;
D O I:
10.1021/ja407589e
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The direct cross-coupling of two different electrophiles, such as an aryl halide with an alkyl halide, offers many advantages over conventional cross-coupling methods that require a carbon nucleophile. Despite its promise as a versatile synthetic strategy, a limited understanding of the mechanism and origin of cross selectivity has hindered progress in reaction development and design. Herein, we shed light on the mechanism for the nickel-catalyzed cross-electrophile coupling of aryl halides with alkyl halides and demonstrate that the selectivity arises from an unusual catalytic cycle that combines both polar and radical steps to form the new C-C bond.
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页码:16192 / 16197
页数:6
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