Morita–Baylis–Hillman (MBH) adducts are versatile starting materials widely employed in
Lewis base catalysis. A myriad of different transformations have been reported based on …

A novel phosphine‐catalyzed, highly enantioselective umpolung addition of trifluoromethyl
ketimines to Morita–Baylis–Hillman carbonates was developed and it provides facile access …

Tandem reactions form two or more new bonds, sequentially and in only one step, avoiding
the purification of each step and the use of protecting groups, thus making them greener …

The β-isocupreidine, a cinchonine derived alkaloid, catalyzed asymmetric SN2′–SN2′
reaction between N-2, 2, 2-trifluoroethylisatin ketimines and MBH type carbonates was …

Mixing of acryloylchloride, dienone 2, N, N-diisopropylethylamine with chiral organocatalyst
5a, which could simultaneously act as Brønsted and Lewis base catalysts, led to a one-pot …

The kinetic data indicate that the addition of tertiary phosphines to α-methylene lactones in
acetic acid is strongly accelerated in comparison to the reactions of related open-chain …

Herein is reported the asymmetric allylic benzylation of Morita–Baylis–Hillman (MBH)
carbonates with 2-methylbenzophenone (MBP) derivatives as nonstabilized photogenerated …

The first asymmetric N‐allylic alkylation of hydrazones with Morita‐Baylis–Hillman (MBH)
carbonates catalyzed by modified Cinchona alkaloids has been developed, affording N …

A series of β-mono-and β, γ-di-substituted α-methylene-γ-lactams was synthesized. This
method involves the 1, 4-addition of nitroalkanes to arylidenemalonates to obtain nitro …

A novel metal-free approach to construct the tetrasubstituted furans from Morita–Baylis–
Hillman (MBH)-carbonates of acetylenic aldehydes has been developed. This strategy …