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Isocyanurate anion radicals via electron-initiated cycloaddition of isocyanates. | LitMetric

Room temperature sodium metal reductions of alkyl isocyanates lead to the rapid electron-initiated formation of alkyl isocyanurate anion radicals, which exhibit EPR coupling to only two equivalent nitrogens. Reduction of (13)C-enriched ethyl isocyanate reveals that the odd electron localizes in the pi system of one carbonyl in the isocyanurate ring. EPR line-width alternation effects indicate that at least two stable conformers are in rapid equilibrium undergoing fast exchange.

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http://dx.doi.org/10.1021/ol801793tDOI Listing

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