One-pot four-component reaction: aqueous TiCl3/PhN2+-mediated alkyl radical addition to imines generated in situ

Org Lett. 2005 Feb 17;7(4):645-8. doi: 10.1021/ol047595d.

Abstract

Ti(III)-induced free-radical decomposition of a phenyldiazonium salt, followed by phenyl radical iodine-atom abstraction from alkyl iodides, leads to a one-pot selective alkyl radical addition to the C-atom of imines generated in situ under aqueous acidic conditions. [reaction: see text]