Visible-light-mediated, nitrogen-centered radical amination of tertiary alkyl halides under metal-free conditions to form α-tertiary amines
2016 ◽
Vol 14
(19)
◽
pp. 4387-4392
◽
Keyword(s):
A mild and operationally convenient amino-functionalization of a range of tertiary alkyl halides that involves a N,N-diiodosulfonamide reactive species has been developed.