623157-98-2Relevant academic research and scientific papers
Silver acetate-catalysed asymmetric 1,3-dipolar cycloadditions of imines and chiral acrylamides
Nyerges, Miklós,Bendell, David,Arany, Andrea,Hibbs, David E.,Coles, Simon J.,Hursthouse, Michael B.,Groundwater, Paul W.,Meth-Cohn, Otto
, p. 3745 - 3753 (2007/10/03)
N-Metallated azomethine ylides were generated by the reaction of arylidene glycine imines with AgOAc and triethylamine. These azomethine ylides undergo cycloaddition to chiral acrylamides with excellent diastereoselectivity. The configuration of two of the cycloadducts was confirmed by X-ray crystallography.
Silver acetate catalysed asymmetric 1,3-dipolar cycloadditions of imines and chiral acrylamides
Nyerges, Miklós,Bendell, David,Arany, Andrea,Hibbs, David E.,Coles, Simon J.,Hursthouse, Michael B.,Groundwater, Paul W.,Meth-Cohn, Otto
, p. 947 - 950 (2007/10/03)
N-Metallated azomethine ylides 5 were generated by the reaction of arylidene glycine imines 1 with AgOAc and triethylamine. These azomethine ylides undergo cycloaddition to chiral acrylamides 2 with excellent diastereoselectivity. The configuration of two
