1056017-60-7Relevant academic research and scientific papers
Enantioselective organocatalytic Michael addition of malonates to α,/β-unsaturated ketones
Li, Pengfei,Wen, Shigang,Yu, Feng,Liu, Qiaoxia,Li, Wenjun,Wang, Yongcan,Liang, Xinmiao,Ye, Jinxing
supporting information; scheme or table, p. 753 - 756 (2009/08/07)
(Chemical Equation Presented) A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-amino (9-deoxy) cinchona alkaloid was developed into asymmetric Michael addition of malonates to enones. A series of cyclic and
A general organocatalytic enantioselective malonate addition to α,β-unsaturated enones
Wascholowski, Veit,Knudsen, Kristian Rahbek,Mitchell, Claire E. T.,Ley, Steven V.
experimental part, p. 6155 - 6165 (2009/05/27)
A general enantioselective organocatalytic conjugate addition procedure of a variety of malonates to α,β-unsaturated enone systems is presented. The reaction is efficiently catalysed by the pyrrolidinyl tetrazole catalyst 1. Cyclic, acyclic and aromatic e
