1152292-51-7Relevant academic research and scientific papers
Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-Morita-Baylis-Hillman reactions at ambient temperature
Garnier, Jean-Marc,Liu, Fei
, p. 1272 - 1275 (2009)
Fast and enantioselective aza-Morita-Baylis-Hillman reactions between electron-deficient or electron-rich aromatic N-tosyl imines and methyl vinyl ketone were achieved at ambient temperature using asymmetric counterion-directed catalysis promoted by trifu
Enantioselective trifunctional organocatalysts for rate-enhanced aza-Morita-Baylis-Hillman reactions at room temperature
Garnier, Jean-Marc,Anstiss, Christopher,Liu, Fei
, p. 331 - 338 (2009)
A Bronsted acid-activated trifunctional organocatalyst, based on the BINAP scaffold, was used for the first time to catalyze aza-Morita-Baylis- Hillman reactions between N-tosylimines and methyl vinyl ketone with fast reaction rates and good enantioselect
Cooperativity in the counterion catalysis of Morita/Baylis/Hillman reactions promoted by enantioselective trifunctional organocatalysts
Anstiss, Christopher,Liu, Fei
experimental part, p. 5486 - 5491 (2010/08/07)
New trifunctional organocatalysts with a NHTs Br?nsted acid were prepared and tested in their ability to promote the counterion catalysis of generic and aza-Morita/Baylis/Hillman reactions.The cooperativity between the counterion and the NHTs Br?nsted aci
