1032429-79-0Relevant articles and documents
A Recyclable Chiral 2-(Triphenylmethyl)pyrrolidine Organocatalyst Anchored to [60]Fullerene
Rosso, Cristian,Emma, Marco G.,Martinelli, Ada,Lombardo, Marco,Quintavalla, Arianna,Trombini, Claudio,Syrgiannis, Zois,Prato, Maurizio
, p. 2936 - 2944 (2019/04/26)
Hybridization of a chiral 3-hydroxy-2-trityl-pyrrolidine deriving from (R)-pyrrolidinol with [60]fullerene via click chemistry provides a highly efficient supported enantioselective organocatalyst, which was successfully exploited in a Michael addition of
Highly enantioselective and recyclable organocatalytic Michael addition of malonates to α,β-unsaturated aldehydes in aqueous media
Ghosh, Subrata K.,Dhungana, Kritanjali,Headley, Allan D.,Ni, Bukuo
, p. 8322 - 8325 (2012/11/07)
A new type of pyrrolidine-based organocatalyst, which was developed earlier in our lab, has been found to be very effective for the Michael addition reaction in aqueous solvents involving a wide range of α,β- unsaturated aldehydes and malonate derivatives
Ionic polymer-supported O-trimethylsilyl-α,α-diphenyl-(S)- prolinols as recoverable organocatalysts for the asymmetric Michael reactions of carbon acids with α,β-enals
Maltsev, Oleg V.,Kucherenko, Alexander S.,Zlotin, Sergei G.
experimental part, p. 146 - 148 (2011/12/22)
A recyclable organocatalyst bearing O-trimethylsilyl-α,α- diphenyl-(S)-prolinol unit tagged to the imidazolium cation and poly(4-styrenesulfonate) anion in the reaction of CH-acids with α,β-enals provided the respective Michael adducts in high yields (up
