107638-86-8Relevant articles and documents
Highly enantioselective Michael addition of cyclic 1,3-dicarbonyl compounds to α,β-unsaturated ketones
Xie, Jian-Wu,Yue, Lei,Chen, Wei,Du, Wei,Zhu, Jin,Deng, Jin-Gen,Chen, Ying-Chun
, p. 413 - 415 (2007)
The highly enantioselective Michael addition of 1,3-cyclic dicarbonyl compounds to α,β-unsaturated ketones was reported to be catalyzed by an organic primary amine derived from quinine. A chiral anticoagulant drug, (S)-warfarin, was directly prepared in 96% ee, and other related important adducts were also obtained in excellent enantioselectivity (89-99% ee).