Abstract
AbstractThe enantioselective oxidative C—H functionalization of tetrahydroisoquinoline derivatives (I) is achieved through the merger of photoredox and asymmetric anion‐binding catalysis.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
