Room temperature hydroamination of alkynes with anilines catalyzed by anti-Bredt di(amino)carbene gold(I) complexes.

The room temp. hydroamination of alkynes with phenylhydrazine and anilines was achieved with an anti-Bredt di(amino) carbene gold(I) chloride as precatalyst, in the presence of KBArF as chloride scavenger. These reactions were highly regioselective and excellent conversions were obtained (up to 99{%}) for a series of alkynes and anilines. [on SciFinder(R)]

Références

Titre
Room temperature hydroamination of alkynes with anilines catalyzed by anti-Bredt di(amino)carbene gold(I) complexes.
Type de publication
Article de revue
Année de publication
2016
Revue
New J. Chem.
Volume
40
Pagination
5993–5996
ISSN
1144-0546
Soumis le 12 avril 2018