Samenvatting
The discovery of an ultrafast cross-coupling of alkyland 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 [C-11]-labeled PET tracer celecoxib.
Originele taal-2 | English |
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Pagina's (van-tot) | 3354-3359 |
Aantal pagina's | 6 |
Tijdschrift | Angewandte Chemie - International Edition |
Volume | 56 |
Nummer van het tijdschrift | 12 |
Vroegere onlinedatum | 14-feb.-2017 |
DOI's | |
Status | Published - 13-mrt.-2017 |