Mn-Mediated Coupling of Alkyl Iodides and Ketimines: A Radical Addition Route to α,α-Disubstituted α-Aminoesters

Friestad, Gregory K.; Ji, An

doi:10.1021/ol800733b.s001

Mn-Mediated Coupling of Alkyl Iodides and Ketimines: A Radical Addition Route to α,α-Disubstituted α-Aminoesters

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posted on 2008-06-05, 00:00 authored by Gregory K. Friestad, An Ji

Coupling of primary and secondary alkyl iodides with N-acylhydrazonoesters via Mn-mediated photolysis conditions affords access to tert-alkyl amines.

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photolysi access alkyl iodides amines Disubstituted Aminoester Radical Addition Route Ketimine Alkyl Iodides

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CC BY-NC 4.0

Mn-Mediated Coupling of Alkyl Iodides and Ketimines: A Radical Addition Route to α,α-Disubstituted α-Aminoesters

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