1089665-77-9Relevant academic research and scientific papers
Novel C2-symmetric phenylglycine derivatives as organocatalysts of the Michael reaction between nitroalkenes and ketones
Kostenko, A. A.,Kucherenko, A. S.,Kuznetsova, O. Yu.,Zlotin, S. G.
, p. 885 - 889 (2021)
A comprehensive study of the activity of the amide-type organocatalysts based on (R)- and (S)-phenylglycine and 1,2-di(2-pyridyl)-1,2-diaminoethane in the asymmetric Michael reaction between various nitroalkenes and ketones was carried out. The products o
A general, highly enantioselective Michael addition of nitroalkanes to α,β-unsaturated enones catalyzed by 9-amino(9-deoxy)-epi-quinine: a remarkable additive effect
Liu, Siyang,Wang, Qingqing,Ye, Ling,Shi, Zhichuan,Zhao, Zhigang,Yang, Xuejun,Ding, Keyi,Li, Xuefeng
supporting information, p. 5115 - 5120 (2016/07/25)
A particularly general protocol for the organocatalytic asymmetric Michael addition of nitroalkanes to α,β-unsaturated enones is reported. The Michael reaction proceeded smoothly and provided the desired adducts in moderate to excellent yields (55–99%) an
