1094570-19-0Relevant articles and documents
Catalytic batch and continuous flow production of highly enantioenriched cyclohexane derivatives with polymer-supported diarylprolinol silyl ethers
Alza, Esther,Sayalero, Sonia,Cambeiro, Xacobe C.,Martín-Rapún, Rafael,Miranda, Pedro O.,Pericàs, Miquel A.
, p. 464 - 468 (2011)
Diarylprolinol silyl ethers immobilized onto polystyrene have been employed as catalysts in the enantioselective domino Michael-Knoevenagel reaction of dimethyl 3-oxoglutarate and 3-substituted acrolein derivatives, including aliphatic ones. The best catalyst allows the preparation of highly functionalized cyclohexane derivatives in a straightforward and efficient manner, both under batch and continuous flow conditions. Georg Thieme Verlag Stuttgart.
Diphenylprolinol silyl ether catalysis in an asymmetric formal carbo [3 + 3] cycloaddition reaction via a domino michael/knoevenagel condensation
Hayashi, Yujiro,Toyoshima, Maya,Gotoh, Hiroaki,Ishikawa, Hayato
supporting information; experimental part, p. 45 - 48 (2009/07/25)
Diphenylprolinol silyl ether was found to catalyze the formal carbo [3 + 3] cycloaddition reaction through the domino reaction via the Michael reaction, followed by Knoevenagel condensation of the α, β-unsaturated aldehyde and dimethyl 3-oxopentanedioate,