The intramolecular additions of C-centered neutral α-aminoalkyl radicals onto suitably positioned C-C double bonds provide a ready access into functionalized carbocycles and heterocycles.This strategy offers considerable versatility in the selection of starting materials since a number of methods using different functional groups and reagents are available for αaminoalkyl radical generation.This review covers the recent progress in this field.
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Aurrecoechea et al. (2004) studied this question.