A C-N bond forming dearomatization protocol with broad scope is outlined. Specifically, bifunctional amino reagents are used for sequential nucleophilic and electrophilic C-N bond formations, with the latter effecting the key dearomatization step. Using this approach, γ-arylated alcohols are converted to a wide range of differentially protected spirocyclic pyrrolidines in just two or three steps.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698738PMC
http://dx.doi.org/10.1002/anie.201708176DOI Listing

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