Termination of Mn(III)-based oxidative cyclizations by trapping with azide

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Abstract

The radicals formed in Mn(III)-based oxidative free-radical cyclizations of β-keto esters and malonate esters can be trapped with sodium azide and Mn(III) to give cyclic and bicyclic azides in 30-80% yield. Reduction of the azide gives bi- and tricyclic lactams.

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Snider, B. B., & Duvall, J. R. (2004). Termination of Mn(III)-based oxidative cyclizations by trapping with azide. Organic Letters, 6(8), 1265–1268. https://doi.org/10.1021/ol049805s

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