Larry E. Overman
Tue, Oct. 2, 2018, 4:30pm
Edward C Taylor Auditorium, Frick B02
Host: David MacMillan
Fragment Coupling with Carbon Radicals
Reactions that allow complex molecular fragments to be combined in high yield occupy an exalted position in organic synthesis because they are fundamental to convergent synthesis strategies. Recent discoveries from our laboratories show that bimolecular reactions of structurally elaborate tertiary carbon radicals and electron-deficient alkenes can unite complex fragments by forming a new sp3–sp3 C–C bond using equimolar amounts of the two coupling partners. Reflecting the large steric bulk of tertiary carbon radicals, these reactions can take place with high stereoselectivity to form new quaternary and secondary carbon stereocenters. Tertiary carbon radicals can be generated conveniently using visible-light photocatalysis, which offers distinct advantages over older less-green methods for forming carbon radicals.