1322722-38-2Relevant academic research and scientific papers
Enantioselective aza-Michael addition to conjugated nitroenynes catalyzed by chiral arylaminophosphonium barfates
Uraguchi, Daisuke,Kinoshita, Natsuko,Kizu, Tomohito,Ooi, Takashi
, p. 1265 - 1267 (2011)
Enantioselective aza-Michael addition to conjugated nitroenynes has been developed. P-Spiro heterochiral arylaminophosphonium barfate 1bBArF effectively catalyzes the reaction, and the corresponding conjugate adducts, β-amino homopropargylic nitro compounds, are obtained in good chemical yields with high enantioselectivities. Georg Thieme Verlag Stuttgart · New York.
