Direct reductive amination of aromatic aldehydes catalyzed by gold(i) complex under transfer hydrogenation conditions
Chemical Communications2011Vol. 47(23), pp. 6605–6605
Citations Over TimeTop 10% of 2011 papers
Abstract
The direct reductive amination of aromatic aldehydes has been achieved with excellent isolated yields (89-96%) using readily accessible Ph(3)PAuCl/AgOTf catalyst along with ethyl Hantzsch ester as hydrogen source under mild reaction conditions.
Related Papers
- → A versatile cobalt catalyst for the reductive amination of carbonyl compounds with nitro compounds by transfer hydrogenation(2017)142 cited
- → Formation of N-Alkylpyrroles via Intermolecular Redox Amination(2009)91 cited
- → One‐Pot Transfer Hydrogenation Reductive Amination of Aldehydes and Ketones by Iridium Complexes “on Water”(2020)30 cited
- → Construction of α-Alkylated Amines by Iridium Complex-Catalyzed One-Step Transfer Hydrogenation of C=C and C=N Bonds(2020)4 cited