A diaminomethylenemalononitrile organocatalyst efficiently catalyzed the asymmetric conjugate addition of α-cyanoketones to vinyl ketones to give the corresponding 1,5-dicarbonyl compounds, which bear an all-carbon quaternary stereogenic center with high enantioselectivities. This report is the first example of the asymmetric conjugate addition of α-cyanoketones to vinyl ketones using an organocatalyst
All-carbon quaternary stereocenters are ubiquitous motifs in biological products and pharmaceutical ...
The copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted cyclic eno...
Organocatalysis is shown to expand the classical reactivity pattern for conjugate addition reactions...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
Herein a comprehensive study is provided on the asymmetric conjugate addition (ACA) of Grignard reag...
The first example of an organocatalytic enantioselective conjugate addition of cyclic beta-ketoester...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
An NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various Grignard reagents to ...
The first effective example of asymmetric conjugate addition–protonation reactions of thiols to α-su...
The catalytic enantioselective conjugate addition of acetaldehyde to polyconjugated substrates, nitr...
Primary amine-salicylamides derived from chiral trans-cyclohexane-1,2-diamines are used as organocat...
The enantioselective organocatalytic conjugate addition of a-aminoketone to nitroolefins is reported
SimplePhos ligands proved to be very powerful ligands in the generation of quaternary stereogenic ce...
α,β-Unsaturated ynones have historically been used as Michael acceptors in conjugate addition reacti...
Dans le domaine de l'addition conjuguée asymétrique sur des enones, un effort considérable a été con...
All-carbon quaternary stereocenters are ubiquitous motifs in biological products and pharmaceutical ...
The copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted cyclic eno...
Organocatalysis is shown to expand the classical reactivity pattern for conjugate addition reactions...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
Herein a comprehensive study is provided on the asymmetric conjugate addition (ACA) of Grignard reag...
The first example of an organocatalytic enantioselective conjugate addition of cyclic beta-ketoester...
The first efficient and highly enantioselective Michael addition–protonation reaction of malononitri...
An NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various Grignard reagents to ...
The first effective example of asymmetric conjugate addition–protonation reactions of thiols to α-su...
The catalytic enantioselective conjugate addition of acetaldehyde to polyconjugated substrates, nitr...
Primary amine-salicylamides derived from chiral trans-cyclohexane-1,2-diamines are used as organocat...
The enantioselective organocatalytic conjugate addition of a-aminoketone to nitroolefins is reported
SimplePhos ligands proved to be very powerful ligands in the generation of quaternary stereogenic ce...
α,β-Unsaturated ynones have historically been used as Michael acceptors in conjugate addition reacti...
Dans le domaine de l'addition conjuguée asymétrique sur des enones, un effort considérable a été con...
All-carbon quaternary stereocenters are ubiquitous motifs in biological products and pharmaceutical ...
The copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted cyclic eno...
Organocatalysis is shown to expand the classical reactivity pattern for conjugate addition reactions...