Taming diamines and acyl chlorides by carbon dioxide in selective mono-acylation reactions
Jerik Mathew Valera Lauridsen, Margarita Poderyte, Jiwoong Lee
Abstract
Selective monoacylation and unsymmetric diamide formation reactions using acyl chlorides and diamines under ambient CO 2 pressure (400 ppm – 1 atm), enabling facile synthesis of bioactive molecules.
Topics & Concepts
AcylationChemistryCarbon dioxideOrganic chemistryMoleculeCombinatorial chemistryCatalysisCarbon dioxide utilization in catalysisAsymmetric Hydrogenation and CatalysisCO2 Reduction Techniques and Catalysts