| Literature DB >> 28194863 |
Dorus Heijnen1, Filippo Tosi1, Carlos Vila1, Marc C A Stuart2, Philip H Elsinga3, Wiktor Szymanski4, Ben L Feringa1.
Abstract
The discovery of an ultrafast cross-coupling of alkyl- and aryllithium reagents with a range of aryl bromides is presented. The essential role of molecular oxygen to form the active palladium catalyst was established; palladium nanoparticles that are highly active in cross-coupling reactions with reaction times ranging from 5 s to 5 min are thus generated in situ. High selectivities were observed for a range of heterocycles and functional groups as well as for an expanded scope of organolithium reagents. The applicability of this method was showcased by the synthesis of the [11 C]-labeled PET tracer celecoxib.Entities:
Keywords: cross-coupling; isotope labeling; nanoparticles; organolithium regents; palladium
Year: 2017 PMID: 28194863 DOI: 10.1002/anie.201700417
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336