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Copper(I)-catalyzed intramolecular addition of N-chloroamines to double bonds under aprotic conditions. Towards a stereoselective catalytic radical reaction
Gottlich
, p. 1561 - 1564 (2000)
Copper(I) complexes catalyze the intramolecular addition of N-chloramines to carbon-carbon double bonds under neutral conditions, a reaction that proceeds via a metal complexed aminyl radical. A high diastereoselectivity is obtained in the cyclization step due to the sterically demanding copper complex.
