Cooperative copper-squaramide catalysis for the enantioselective N-H insertion reaction with sulfoxonium ylides.

ABSTRACT: The first examples of a highly efficient and enantioselective carbene-mediated insertion reaction, from a sulfur ylide, are described. By way of a catalytic asymmetric insertion reaction into N-H bonds from carbonyl sulfoxonium ylides and anilines, using a copper-bifunctional squaramide cooperative catalysis approach, thirty-seven α-arylglycine esters were synthesized in enantiomeric ratios up to 92 : 8 (99 : 1 after a single recrystallization) and reaction yields ranging between 49-96%. Furthermore, the protocol benefits from quick reaction times and is conducted in a straightforward manner.

SUBMITTER: Furniel LG 

PROVIDER: S-EPMC8171336 | biostudies-literature |

REPOSITORIES: biostudies-literature