Metallaphotoredox: The Merger of Photoredox and Transition Metal Catalysis

被引:957
|
作者
Chan, Amy Y. [1 ]
Perry, Ian B. [1 ]
Bissonnette, Noah B. [1 ]
Buksh, Benito F. [1 ]
Edwards, Grant A. [1 ]
Frye, Lucas, I [1 ]
Garry, Olivia L. [1 ]
Lavagnino, Marissa N. [1 ]
Li, Beryl X. [1 ]
Liang, Yufan [1 ]
Mao, Edna [1 ]
Millet, Agustin [1 ]
Oakley, James, V [1 ]
Reed, Nicholas L. [1 ]
Sakai, Holt A. [1 ]
Seath, Ciaran P. [1 ]
MacMillan, David W. C. [1 ]
机构
[1] Princeton Univ, Merck Ctr Catalysis, Princeton, NJ 08544 USA
关键词
VISIBLE-LIGHT PHOTOREDOX; C-H ARYLATION; CROSS-COUPLING REACTIONS; SINGLE-ELECTRON TRANSMETALATION; HYDROGEN-ATOM TRANSFER; ALPHA-AMINO-ACIDS; MERGING PHOTOREDOX; CARBOXYLIC-ACIDS; DUAL CATALYSIS; OXIDATIVE ADDITION;
D O I
10.1021/acs.chemrev.1c00383
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The merger of photoredox catalysis with transition metal catalysis, termed metallaphotoredox catalysis, has become a mainstay in synthetic methodology over the past decade. Metallaphotoredox catalysis has combined the unparalleled capacity of transition metal catalysis for bond formation with the broad utility of photoinduced electron- and energy-transfer processes. Photocatalytic substrate activation has allowed the engagement of simple starting materials in metal-mediated bond-forming processes. Moreover, electron or energy transfer directly with key organometallic intermediates has provided novel activation modes entirely complementary to traditional catalytic platforms. This Review details and contextualizes the advancements in molecule construction brought forth by metallaphotocatalysis.
引用
收藏
页码:1485 / 1542
页数:58
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