Add to ORKGL-Proline derived spirolactams and a-methyl prolinamides act as organocatalysts for the asymmetric conjugate addition of aldehydes to nitroolefins in excellent yields, with good diastereoselectivity and enantioselectivity. Furthermore, low catalyst loadings (5 mol%) and a low aldehyde molar excess (1.5 molar equivalents) were achieved
A class of ionic liquid supported (ILS) (S)-pyrrolidine sulfonamide organocatalyst (1c), which was d...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
In recent years there has been a dynamic development of asymmetric synthesis. Groups of researchers,...
WOS:000302663700010The asymmetric Michael addition of aldehydes to nitroolefins was investigated usi...
The asymmetric Michael addition of aldehydes to nitroolefins was investigated using L-prolinamide de...
The development of organocatalysts for asymmetric synthesis continues to be actively investigated in...
Different L-prolinamides 21, prepared from L-proline and chiral β-amino alcohols are active bifunct...
At the beginning of the 21st century, organocatalysis has emerged as a new powerful methodology for ...
Chiral, polysubstituted proline esters, obtained via cycloaddition reactions of azomethine ylides, w...
(S)-Binam-L-prolinamide (20 mol%) catalyze the enantioselective Michael addition of several α-alkoxy...
The organocatalytic Michael addition of aldehydes to ketones is of continuing interest in developmen...
Four 2-(trifluoromethylsulfonamidoalkyl)pyrrolidines and their d-prolinamides were prepared and scr...
The efficiency of an amino imidate organocatalyst was evaluated in the Michael reaction of ketones w...
New pyrrolidine-based organocatalysts with a bulky substituent at C2 were synthesized from chiral im...
Various l-prolinamides 14, prepared from l-proline and chiral β-amino alcohols, are active bifunctio...
A class of ionic liquid supported (ILS) (S)-pyrrolidine sulfonamide organocatalyst (1c), which was d...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
In recent years there has been a dynamic development of asymmetric synthesis. Groups of researchers,...
WOS:000302663700010The asymmetric Michael addition of aldehydes to nitroolefins was investigated usi...
The asymmetric Michael addition of aldehydes to nitroolefins was investigated using L-prolinamide de...
The development of organocatalysts for asymmetric synthesis continues to be actively investigated in...
Different L-prolinamides 21, prepared from L-proline and chiral β-amino alcohols are active bifunct...
At the beginning of the 21st century, organocatalysis has emerged as a new powerful methodology for ...
Chiral, polysubstituted proline esters, obtained via cycloaddition reactions of azomethine ylides, w...
(S)-Binam-L-prolinamide (20 mol%) catalyze the enantioselective Michael addition of several α-alkoxy...
The organocatalytic Michael addition of aldehydes to ketones is of continuing interest in developmen...
Four 2-(trifluoromethylsulfonamidoalkyl)pyrrolidines and their d-prolinamides were prepared and scr...
The efficiency of an amino imidate organocatalyst was evaluated in the Michael reaction of ketones w...
New pyrrolidine-based organocatalysts with a bulky substituent at C2 were synthesized from chiral im...
Various l-prolinamides 14, prepared from l-proline and chiral β-amino alcohols, are active bifunctio...
A class of ionic liquid supported (ILS) (S)-pyrrolidine sulfonamide organocatalyst (1c), which was d...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
In recent years there has been a dynamic development of asymmetric synthesis. Groups of researchers,...