Multimetallic-Catalyzed C-C Bond-Forming Reactions: From Serendipity to Strategy

被引:31
|
作者
Ackerman-Biegasiewicz, Laura K. G. [1 ]
Kariofillis, Stavros K. [2 ,3 ]
Weix, Daniel J. [4 ]
机构
[1] Arizona State Univ, Sch Mol Sci, Dept Chem, Tempe, AZ 85281 USA
[2] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
[3] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[4] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
CHAIN-TRANSFER POLYMERIZATION; BIMETALLIC CATALYSIS; COUPLING REACTIONS; DIRECT ARYLATION; COOPERATIVE CATALYSIS; REDUCTIVE ELIMINATION; PHOTOREDOX CATALYSIS; OXIDATIVE ADDITION; TANDEM CATALYSIS; METAL-COMPLEXES;
D O I
10.1021/jacs.2c08615
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The use of two or more metal catalysts in a reaction is a powerful synthetic strategy to access complex targets efficiently and selectively from simple starting materials. While capable of uniting distinct reactivities, the principles governing multimetallic catalysis are not always intuitive, making the discovery and optimization of new reactions challenging. Here, we outline our perspective on the design elements of multimetallic catalysis using precedent from well-documented C-C bond-forming reactions. These strategies provide insight into the synergy of metal catalysts and compatibility of the individual components of a reaction. Advantages and limitations are discussed to promote further development of the field.
引用
收藏
页码:6596 / 6614
页数:19
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