Abstract
Lithium perchlorate was highly concentrated on the polyethyleneglycol modified electrode and promoted Diels-Alder reactions. By using the modified electrode in acetonitrile, hydroquinones were efficiently oxidized to corresponding quinones which were immediately trapped by dienes to give varied cycloadducts.
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References
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© 1998 Springer Japan
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Chiba, K., Kim, S., Tada, M. (1998). Diels-Alder Reaction of in Situ Generated Quinones on a Lithium Perchlorate/Polyethyleneglycol Modified Electrode. In: Torii, S. (eds) Novel Trends in Electroorganic Synthesis. Springer, Tokyo. https://doi.org/10.1007/978-4-431-65924-2_54
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DOI: https://doi.org/10.1007/978-4-431-65924-2_54
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