Mechanistic study of the bismuth mediated fluorination of arylboronic esters and further rational design.

ABSTRACT: Density functional theory (DFT) calculations have been performed to gain insight into the catalytic mechanism of the bismuth redox catalyzed fluorination of arylboronic esters to deliver the widely used arylfluoride compounds (Science 2020, 367, 313-317). The study reveals that the whole catalysis can be characterized via three stages: (i) transmetallation generates the Bi(iii) intermediate 5, capitalizing on the use of KF as an activator. (ii) 5 then reacts with the electrophilic fluorination reagent 1-fluoro-2,6-dichloropyridinium 4via oxidative addition to give the Bi(v) intermediate IM4A. (iii) IM4A undergoes a reductive elimination step to yield aryl fluoride compounds and regenerates the bismuth catalyst for the next catalytic cycle. Each stage is kinetica

SUBMITTER: Cai J 

PROVIDER: S-EPMC9404455 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature