Transition Metal‐Catalyzed C−H Functionalization Through Electrocatalysis
Electrochemically promoted transition metal‐catalyzed C−H functionalization has emerged as a promising area of research over the last few decades. However, development in this field is still at an early stage compared to traditional functionalization reactions using chemical‐based oxidizing agents....
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Published in: | ChemSusChem Vol. 16; no. 12; pp. e202202201 - n/a |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Germany
Wiley Subscription Services, Inc
22-06-2023
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Subjects: | |
Online Access: | Get full text |
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Summary: | Electrochemically promoted transition metal‐catalyzed C−H functionalization has emerged as a promising area of research over the last few decades. However, development in this field is still at an early stage compared to traditional functionalization reactions using chemical‐based oxidizing agents. Recent reports have shown increased attention on electrochemically promoted metal‐catalyzed C−H functionalization. From the standpoint of sustainability, environmental friendliness, and cost effectiveness, electrochemically promoted oxidation of a metal catalyst offers a mild, efficient, and atom‐economical alternative to traditional chemical oxidants. This Review discusses advances in the field of transition metal‐electrocatalyzed C−H functionalization over the past decade and describes how the unique features of electricity enable metal‐catalyzed C−H functionalization in an economic and sustainable way.
Merging transition metal catalysis with electrochemical oxidation has emerged as a potential catalyst system for C−H bond functionalization, avoiding the use of chemical‐based oxidants. Electrochemically promoted electrooxidation of the metal catalyst offers a mild, efficient and atom‐economical alternative to traditional chemical oxidant‐based systems. This Review highlights recent advances in transition metal‐electrocatalyzed C−H functionalization reactions. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1864-5631 1864-564X |
DOI: | 10.1002/cssc.202202201 |