【摘 要】
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Organic electrosynthesis has been widely used as an environmentally conscious alternative to conven-tional methods for redox reactions because it utilizes electric current as a traceless redox agent instead of chemical redox agents.Indirect electrolysis e
【机 构】
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State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,University
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Organic electrosynthesis has been widely used as an environmentally conscious alternative to conven-tional methods for redox reactions because it utilizes electric current as a traceless redox agent instead of chemical redox agents.Indirect electrolysis employing a redox catalyst has received tremendous atten-tion,since it provides various advantages compared to direct electrolysis.With indirect electrolysis,over-potential of electron transfer can be avoided,which is inherently milder,thus wide functional group tolerance can be achieved.Additionally,chemoselectivity,regioselectivity,and stereoselectivity can be tuned by the redox catalysts used in indirect electrolysis.Furthermore,electrode passivation can be avoided by preventing the formation of polymer films on the electrode surface.Common redox catalysts include N-oxyl radicals,hypervalent iodine species,halides,amines,benzoquinones(such as DDQ and tetrachlorobenzoquinone),and transition metals.In recent years,great progress has been made in the field of indirect organic electrosynthesis using transition metals as redox catalysts for reaction classes including C-H functionalization,radical cyclization,and cross-coupling of aryl halides-each owing to the diverse reactivity and accessible oxidation states of transition metals.Although various reviews of organic electrosynthesis are available,there is a lack of articles that focus on recent research progress in the area of indirect electrolysis using transition metals,which is the impetus for this review.
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