1203648-35-4Relevant academic research and scientific papers
Asymmetric Michael reactions catalyzed by a highly efficient and recyclable quaternary ammonium ionic liquid-supported organocatalyst in aqueous media
Ghosh, Subrata K.,Qiao, Yupu,Ni, Bukuo,Headley, Allan D.
, p. 1801 - 1804 (2013)
A novel ionic liquid-support organocatalyst, which contains the quaternary ammonium ion moiety, was recently developed and successfully applied to the asymmetric Michael reaction in the presence of a newly developed ionic liquid-supported (ILS) benzoic ac
A novel recyclable organocatalytic system for the highly asymmetric michael addition of aldehydes to nitroolefins in water
Sarkar, Dhruba,Bhattarai, Ramesh,Headley, Allan D.,Ni, Bukuo
experimental part, p. 1993 - 1997 (2011/08/05)
A novel strategy for the asymmetric Michael addition of aldehydes to nitroolefins with a catalytic system of organocatalyst 1 in combination with ionic-liquid-supported (ILS) benzoic acid in water has been developed. The Michael adducts of this system giv
Diarylprolinol silyl ether salts as new, efficient, water-soluble, and recyclable organocatalysts for the asymmetric michael addition on water
Zheng, Zilong,Perkins, Benjamin L.,Ni, Bukuo
supporting information; experimental part, p. 50 - 51 (2010/03/25)
(Chemical Equation Presented) A novel strategy for the catalytic asymmetric Michael addition of aldehydes to nitroolefins on water has been developed and provided the Michael adducts in excellent diastereo- and enantioselectivities. A notable feature of t
