Considering organic mechanisms and the optimization of current flow in an electrochemical oxidative condensation reaction

Literature Information

Publication Date 2016-07-05
DOI 10.1039/C6QO00248J
Impact Factor 5.281
Authors

Derek T. Rensing, Bichlien H. Nguyen, Kevin D. Moeller


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Abstract

Oxidative condensation reactions are potentially valuable tools for the valorization of lignin derived materials. They are used in the two step conversion of raw sawdust into benzothiazole and benzimidazole ring skeletons. The reactions are also excellent candidates for use in paired electrochemical reactions that utilize the cathodic half-reaction to make the hydrogen gas needed for the conversion of lignin derived materials into indanones. However, the optimized oxidative condensation reactions used to date require the use of low currents that inhibit their utility in paired electrochemical reactions. In this manuscript, the optimization of current for the oxidative condensation is examined and this optimization is used to illustrate how the optimization of an electrochemical reaction relies on a traditional look at organic mechanisms.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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