Origins of high catalyst loading in copper(i)-catalysed Ullmann-Goldberg C-N coupling reactions.

ABSTRACT: A mechanistic investigation of Ullmann-Goldberg reactions using soluble and partially soluble bases led to the identification of various pathways for catalyst deactivation through (i) product inhibition with amine products, (ii) by-product inhibition with inorganic halide salts, and (iii) ligand exchange by soluble carboxylate bases. The reactions using partially soluble inorganic bases showed variable induction periods, which are responsible for the reproducibility issues in these reactions. Surprisingly, more finely milled Cs₂CO₃ resulted in a longer induction period due to the higher concentration of the deprotonated amine/amide, leading to suppressed catalytic activity. These results have significant implications on future ligand development for the Ullmann-Goldbe

SUBMITTER: Sherborne GJ 

PROVIDER: S-EPMC5688446 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature