1152292-52-8Relevant academic research and scientific papers
Planar chiral [2.2]paracyclophane-based phosphine-Bronsted acid catalysts bearing exceptionally high reactivity for aza-Morita-Baylis-Hillman reaction
Kitagaki, Shinji,Ohta, Yuu,Takahashi, Ryohei,Komizu, Mika,Mukai, Chisato
supporting information, p. 384 - 386 (2013/02/25)
Several new planar chiral bifunctional phosphine compounds based on the [2.2]paracyclophane backbone with a pseudo-ortho substitution pattern have been synthesized and applied to the aza-Morita-Baylis-Hillman reaction. An enantiopure phosphine-phenol cata
Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-Morita-Baylis-Hillman reactions at ambient temperature
Garnier, Jean-Marc,Liu, Fei
experimental part, p. 1272 - 1275 (2009/10/23)
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
experimental part, p. 331 - 338 (2009/11/30)
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
