N-Metallated azomethine ylides 5 were generated by the reaction of arylidene glycine imines 1 with AgOAc and triethylamine. These azomethine ylides undergo cycloaddition to chiral acrylamides 2 with excellent diastereoselectivity. The configuration of two of the cycloadducts (3a(1) and 3c(1)) has been confirmed by Xray crystallography
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
The first catalytic asymmetric inverse electron demand 1,3-dipolar cycloaddition of azomethine imine...
The preparation of two enantiomerically enriched amino lactones as chiral starting substrates for as...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
Upon treatment with triethylamine or DBU in the presence of LiBr, aromatic and aliphatic imines of a...
In this study new twelve phosphorus based chiral ligands were synthesized and characterized. Then th...
A new chiral aziridino alcohol ligand for zinc(II)-catalyzed azomethine ylide cycloadditions is desc...
The reaction of azomethine ylide 1,3-dipoles with olefinic dipo-larophiles forms highly substituted ...
A protocol to access useful 4-aminopyrrolidine-2,4-dicarboxylate derivatives has been developed. A v...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
The enantioselective binap–silver catalyzed multicomponent 1,3-dipolar cycloaddition using ethyl gly...
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddit...
Enantiopure fluorinated prolines with four chiral centers were obtained from 1,3-dipolar cycloadditi...
The silver-catalysed multicomponent reaction between ethyl glyoxylate, 2,2-dimethoxyacetaldehyde, or...
Pyrrolidine skeleton can be found as core structures in many natural compounds. Almost all pyrrolidi...
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
The first catalytic asymmetric inverse electron demand 1,3-dipolar cycloaddition of azomethine imine...
The preparation of two enantiomerically enriched amino lactones as chiral starting substrates for as...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
Upon treatment with triethylamine or DBU in the presence of LiBr, aromatic and aliphatic imines of a...
In this study new twelve phosphorus based chiral ligands were synthesized and characterized. Then th...
A new chiral aziridino alcohol ligand for zinc(II)-catalyzed azomethine ylide cycloadditions is desc...
The reaction of azomethine ylide 1,3-dipoles with olefinic dipo-larophiles forms highly substituted ...
A protocol to access useful 4-aminopyrrolidine-2,4-dicarboxylate derivatives has been developed. A v...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
The enantioselective binap–silver catalyzed multicomponent 1,3-dipolar cycloaddition using ethyl gly...
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddit...
Enantiopure fluorinated prolines with four chiral centers were obtained from 1,3-dipolar cycloadditi...
The silver-catalysed multicomponent reaction between ethyl glyoxylate, 2,2-dimethoxyacetaldehyde, or...
Pyrrolidine skeleton can be found as core structures in many natural compounds. Almost all pyrrolidi...
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
The first catalytic asymmetric inverse electron demand 1,3-dipolar cycloaddition of azomethine imine...
The preparation of two enantiomerically enriched amino lactones as chiral starting substrates for as...