2006
DOI: 10.1016/j.tetlet.2006.01.113
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CO2 anion–radical in organic carboxylations

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Cited by 46 publications
(12 citation statements)
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“…This reaction setup was also tested with propionitrile, butyronitrile, benzyl chloride and toluene in the anolyte compartment. Adjacent functional groups weaken C–H bonds, yielding relatively stable radicals, in turn resulting in selective CO 2 fixation [ 150 ].…”
Section: Reviewmentioning
confidence: 99%
“…This reaction setup was also tested with propionitrile, butyronitrile, benzyl chloride and toluene in the anolyte compartment. Adjacent functional groups weaken C–H bonds, yielding relatively stable radicals, in turn resulting in selective CO 2 fixation [ 150 ].…”
Section: Reviewmentioning
confidence: 99%
“…Therefore, they constitute most promising carbon-based energy vectors derived from this value-added carbon management technology. As the electrochemical method offers several advantages 101 over thermochemical routes a great variety of organic compounds such as benzylchlorides, 182,183 alkenes, 184 alkynes and epoxides, 185,186 have been successfully synthesized by electrochemical routes.…”
Section: Electrochemical Co 2 Conversionmentioning
confidence: 99%
“…It should be noted that reduction of CO 2 to formate was the main process observed if the nickel catalyst was omitted and only the ruthenium complex was used [11]. Closely related systems have been exploited also for photoreduction processes on substrates different from CO 2 , such as the reductive dehalogenation of organic halides [22].…”
Section: Introductionmentioning
confidence: 99%