Electroreductive coupling of vinylpyridines and vinylquinolines: radical anion–substrate cycloaddition?
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Robert G. Janssen and Majid Motevalli
Abstract
Cathodic reduction of 2- and 4-vinylpyridine and of 2-vinylquinoline gives trans-1,12-di(heteroaryl)cyclobutanes as major products; they arise via radical anion–substrate cycloaddition.
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Formal reduction potentials (E°) were measured in collaboration with
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Copenhagen).
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