3d metallaelectrocatalysis for resource economical syntheses

被引:171
作者
Gandeepan, Parthasarathy [1 ,2 ]
Finger, Lars H. [1 ]
Meyer, Tjark H. [1 ]
Ackermann, Lutz [1 ,3 ,4 ]
机构
[1] Georg August Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-37077 Gottingen, Germany
[2] Indian Inst Technol Tirupati, Dept Chem, Tirupati 517506, Andhra Pradesh, India
[3] Georg August Univ Gottingen, Woehler Res Inst Sustainable Chem WISCh, Tammannstr 2, D-37077 Gottingen, Germany
[4] Univ Pavia, Dept Chem, Viale Taramelli 10, I-27100 Pavia, Italy
关键词
C-H ACTIVATION; NICKEL-CATALYZED AMINATION; CROSS-COUPLING REACTIONS; BOND FUNCTIONALIZATION; ASYMMETRIC DIHYDROXYLATION; OXIDASE CATALYSIS; ATOM ECONOMY; ARYL HALIDES; PALLADIUM; OLEFINS;
D O I
10.1039/d0cs00149j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Resource economy constitutes one of the key challenges for researchers and practitioners in academia and industries, in terms of rising demand for sustainable and green synthetic methodology. To achieve ideal levels of resource economy in molecular syntheses, novel avenues are required, which include, but are not limited to the use of naturally abundant, renewable feedstocks, solvents, metal catalysts, energy, and redox reagents. In this context, electrosyntheses create the unique possibility to replace stoichiometric amounts of oxidizing or reducing reagents as well as electron transfer events by electric current. Particularly, the merger of Earth-abundant 3d metal catalysis and electrooxidation has recently been recognized as an increasingly viable strategy to forge challenging C-C and C-heteroatom bonds for complex organic molecules in a sustainable fashion under mild reaction conditions. In this review, we highlight the key developments in 3d metallaelectrocatalysis in the context of resource economy in molecular syntheses until February 2020.
引用
收藏
页码:4254 / 4272
页数:19
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