Data from: Access to SCF3 substituted indolizines via a photocatalytic late-stage functionalization protocol

A mild, scalable, and highly chemoselective photocatalytic method was
developed for the direct indolizine functionalization with
N-((trifluoromethyl)thio)saccharin, yielding high amounts of desired
products while tolerating various functional groups. The photoredox
catalyst employed offers a straightforward and inexpensive alternative to
commercially available catalysts. Additionally, a 3-SCF₃ analogue of a
histamine H3 receptor antagonist was synthesized with excellent yield,
demonstrating the strategy’s potential in developing biologically relevant
molecules.