Abstract

AbstractChiral indoline–benzodiazepines were synthesized via an enantioselective Pictet–Spengler‐type reaction catalyzed by chiral imidodiphosphoric acids. A variety of substitution patterns were achieved at room temperature by using 5 mol % catalysts with high yields (up to 97 %) and enantioselectivities (up to 99 % ee).

Full Text
Published version (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