Gold-Catalyzed Hydroarylation of Alkenes with Dialkylanilines.

Anti-Bredt di(amino)carbene supported gold(I) chloride complexes are readily prepd. in two steps from the corresponding isocyanide complexes. In the presence of KB(C6F5)4 as chloride scavenger, they promote the unprecedented hydroarylation reaction of alkenes, e.g., $\alpha$-methylsytyrene, with N,N-dialkylanilines, e.g., N,N-dimethylaniline, with high para-selectivity. The latter are challenging arenes for Friedel-Craft reactions, due to their high basicity. [on SciFinder(R)]

Références

Titre
Gold-Catalyzed Hydroarylation of Alkenes with Dialkylanilines.
Type de publication
Article de revue
Année de publication
2014
Revue
J. Am. Chem. Soc.
Volume
136
Pagination
13594–13597
ISSN
0002-7863
Soumis le 21 janvier 2019