Gould / M. J. J. Pharm / Merck / Norton / Amgen / Lotus Separations LLC / Gaussian Inc. / Sieber S. A. / Wayner D. D. / MacMillan / ASSOCIATED CONTENT / /
Country
Germany / United States / United Kingdom / / /
Facility
Princeton University / /
IndustryTerm
aldehyde products / α-amino aldehyde product / αamination protocol / diverse α-amino aldehyde products / electrophilic radical systems / base-sensitive products / chemical correlation / electronrich reaction site / αdialkyl aldehyde systems / crude product / enantioselective applications / /
Organization
David W. C. MacMillan* Merck Center for Catalysis / German Academic Exchange Service / Princeton University / /
Person
Jennifer L. Alleva / Christian M. König / Giuseppe Cecere / Foley / /
Position
rt rt rt rt rt / representative / AUTHOR INFORMATION Corresponding Author dmacmill@princeton.edu Notes The authors / /
Communication pubs.acs.org/JACS Enantioselective Direct α‑Amination of Aldehydes via a Photoredox Mechanism: A Strategy for Asymmetric Amine Fragment Coupling Giuseppe Cecere, Christian M. König, Jennifer L. Alleva,