Photochemical Decarboxylative Radical Alkylation/Cyclization Reaction to Fused Nitrogen Heterocycles by <scp>LiI</scp>/<scp>PPh<sub>3</sub></scp> Catalysis
Jia‐Li Sui, Xin‐Qian Liu, S. Li, Peng‐Fei Huang, Yu Liu, Jin‐Heng Li
Abstract
Comprehensive Summary A visible‐light‐induced decarboxylative radical cascade cyclization reaction between N ‐(2‐cyanoaryl)‐acrylamides and alkyl N ‐(acyloxy)phthalimide (NHPI esters) for the construction of phenanthridine derivatives has been developed. This approach utilizes lithium iodide (LiI) and triphenylphosphine (PPh 3 ) as the redox catalysts and the alkyl radical is produced through the photoactivation of the electron donor‐acceptor (EDA) complex. A series of primary, secondary, and tertiary alkyl‐substituted phenanthridines are prepared in up to 82% yield without transition‐metal catalysts, chemical oxidants, or metal‐/organic dye‐based photocatalysts.
Topics & Concepts
ChemistryCatalysisAlkylationNitrogenDecarboxylationMedicinal chemistryOrganic chemistryPhotochemistryCatalytic C–H Functionalization MethodsRadical Photochemical ReactionsSulfur-Based Synthesis Techniques