125506-40-3Relevant academic research and scientific papers
Intermolecular mono-and dihydroamination of activated alkenes using a recoverable gold catalyst
Medina, Florian,Michon, Christophe,Agbossou-Niedercorn, Francine
supporting information, p. 6218 - 6227 (2013/01/15)
A combination of gold chloride organometallic complex and a silver salt was used to catalyze intermolecular hydroamination of activated alkenes, i.e aza-Michael reactions. The gold-catalyzed reactions of activated alkenes with nitrogen substrates were investigated and found to afford various mono-and dihydroamination products, the latter being rare and original. After flash chromatography, gold NHC catalyst could be recovered as a gold hydroxide NHC complex. When combined with a silver salt, the gold complex lead again to an active hydroamination catalyst.
1,4-Addition of (Diphenylmethylene)amine to Acceptor Substituted Olefins. A Versatile Synthesis of Protected β-Amino Acids, Nitriles, and Ketones
Wessjohann, Ludger,McGaffin, Gregory,Meijere, Armin de
, p. 359 - 363 (2007/10/02)
(Diphenylmethylene)amine cleanly reacts with a variety of α,β-unsaturated esters, nitriles, ketones, and aldehydes 1a-q to give Michael type adducts 2a-q, generally, in respectable to excellent yields.Sterically congested and donor-substituted Michael acceptors do not react.The β-amino-substituted products can be further transformed in their protected form, or selectively deprotected under mild conditions, e.g. by catalytic hydrogenation.
