4.4 Review

Applications of Proton-Coupled Electron Transfer in Organic Synthesis

Journal

CHINESE JOURNAL OF ORGANIC CHEMISTRY
Volume 41, Issue 10, Pages 3844-3879

Publisher

SCIENCE PRESS
DOI: 10.6023/cjoc202106001

Keywords

proton-coupled electron transfer; organic synthesis; radical reactions; functionalization

Funding

  1. Startup Fund from Nankai University

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Proton-coupled electron transfer (PCET) reactions are unconventional redox reactions with special reactivities and selectivities due to their unique interdependent electron-proton transfer mechanisms. These reactions play a key role in organic synthesis, and through electrochemical and photochemical methods, various activation reactions have been achieved, leading to the synthesis of important structures and fundamental frameworks.
Proton-coupled electron transfer (PCET) reactions are a kind of unconventional redox reactions, which exhibit special reactivities and selectivities due to their unique interdependent electron-proton transfer mechanisms. There are three possible pathways of PCET processes, including stepwise electron transfer followed by proton transfer (ETPT), proton transfer followed by electron transfer (PTET), and concerted pathway in which electron and proton transfer synchronously (CEPT), avoiding intermediates with high energy. These reactions have been playing a key role in numerous areas in organic chemistry, inorganic chemistry, bioorganic chemistry, organometallic and material chemistry, including the redox processes in natural and artificial systems, such as the activation for small molecules. Recently, the application of PCET reactions in organic synthesis has received a great deal of attentions and interests. Being accompanied by the development of electrochemical methods and photocatalysts, more and more novel reactions in electrochemistry and photochemistry involve PCET processes have been reported. Applying these electrochemical and photochemical methods, the activation of X-H bond has been achieved via PCET processes, including C-H bond, N-H bond, P-H bond, S-H bond or O-H bond. Thus, based on these crucial processes, a number of vital structures and fundamental frameworks can be synthesized, and various synthetic building blocks and natural products have been attained. For example, pharmaceutical building blocks like 2 degrees-piperidines can be cyanated at their a-position; substituted dimeric pyrroloindolines such as (-)-calycanthidine, (-)-chimonanthine, and (-)-psychotriasine have also been successfully synthesized via PCET mechanism. Moreover, not only the products of reduction of multiple bonds (C= Y bond such as C=C bond, C=N bond and C=O bond), but also the products of self/cross-coupling have been achieved via PCET mechanism. In this review, the recent applications and developments of PCET mechanism in organic synthesis are summarized, including new catalyst systems and new reagents, especially with electrochemical and photochemical methodologies. The future of this area has also been demonstrated from both experimental and theoretical aspects.

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