A nickel-catalyzed reductive cross-coupling between aziridines and benzyl chlorides has been developed. This method provides direct access to β-benzyl-substituted arylethylamines and enables their conversion to tetrahydroisoquinoline derivatives.
Aziridine is a fascinating core which enables synthesis of diverse N-heterocycles comprising natural product analogs and pharmaceutical candidates.
This review explores MOFs, COFs, and POPs as advanced framework materials for the efficient conversion of CO2 into bioactive oxazolidinones.
This paper reviews progress in the photochemical/electrochemical construction of heterocyclic compounds using CO2, differentiating between various reaction types and elucidating their underlying mechanisms as well as potential applications.
Enantioenriched alkynyl-substituted 1,2-diamines and 2-ethynylaziridines were obtained via catalytic kinetic resolution of racemic aziridines.