National Laboratory of Translational Neuroscience(RRF-2.3.1-21-2022-00015)
Nemzeti Gyógyszerkutatási és Fejlesztési Laboratórium(PharmaLab) Támogató: NKFIH
Szakterületek:
Kémiai tudományok
In this study, we describe the synthesis of cinchona (thio)squaramide and a novel
cinchona thiourea organocatalyst. These catalysts were employed in pharmaceutically
relevant catalytic asymmetric reactions, such as Michael, Friedel–Crafts, and A 3
coupling reactions, in combination with Ag(I), Cu(II), and Ni(II) salts. We identified
several organocatalyst‐metal salt combinations that led to a significant increase
in both yield and enantioselectivity. To gain insight into the active catalyst species,
we prepared organocatalyst‐metal complexes and characterized them using HRMS, NMR
spectroscopy, and quantum chemical calculations (B3LYP‐D4/def2‐TZVP), which allowed
us to establish a structure‐activity relationship.