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Synlett 2005(2): 275-278
DOI: 10.1055/s-2004-837205
DOI: 10.1055/s-2004-837205
LETTER
© Georg Thieme Verlag Stuttgart · New York
Buchwald-Hartwig Aminations of Aryl Chlorides: A Practical Protocol Based on Commercially Available Pd(0)-NHC Catalysts
Weitere Informationen
Received
15 October 2004
Publikationsdatum:
17. Dezember 2004 (online)
Publikationsverlauf
Publikationsdatum:
17. Dezember 2004 (online)
Abstract
Commercially available, air- and water-stable naphthoquinone imidazolin-2-ylidene-palladium(0) complexes were found to be highly active one-component catalysts for the amination of aryl halides. With these very robust catalysts, the expensive bases Cs2CO3 or NaOt-Bu traditionally used can be replaced by KOH. A convenient reaction protocol has been developed for the coupling of a wide range of aryl chlorides with primary or secondary amines.
Key words
carbene ligands - amination - palladium - aryl chlorides
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