The asymmetric Strecker reaction of aldimines and trimethylsilyl cyanide promoted by 1 equivalent of chiral N-oxide affords the corresponding a-amino nitriles with enantioselectivities of Up to 73% most effectively for electron-deficient aldimines under mild reaction conditions. Two new resolving methods and one new synthetic methodology were developed to obtain three novel chiral N-oxides
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
International audienceOptically active .alpha.-amino nitriles and .alpha.-amino phosphinic derivs. h...
A simple, convenient, and practical method for the synthesis of alpha-amino nitriles through a one-p...
Axially chiral N,N'-dioxide Lewis base promoters have been developed and have for the first time bee...
none4noThe synthesis of a series of new chiral alpha-aminonitriles was achieved in a diastereoselect...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...
A simple and novel chiral amide-based organocatalyst <b>6</b> was synthesized from readily available...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
An organocatalytic enantioselective Strecker reaction for the synthesis of 3-amino-3-cyanooxindoles ...
Gröger H, Asano Y. Cyanide-Free Enantioselective Catalytic Strategies for the Synthesis of Chiral Ni...
The first organocatalytic asymmetric three-component Strecker reaction, the urea-catalyzed acylcyana...
Enantioselective synthesis of α-perfluoroalkylated cyclic amino acids and their derivatives was elab...
In summary, this work deals with the enantioselective synthesis of - and -amino nitriles, which can ...
A series of α-quaternary arylglycines were prepared in high optical purity (up to 98% ee) by α-alkyl...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
International audienceOptically active .alpha.-amino nitriles and .alpha.-amino phosphinic derivs. h...
A simple, convenient, and practical method for the synthesis of alpha-amino nitriles through a one-p...
Axially chiral N,N'-dioxide Lewis base promoters have been developed and have for the first time bee...
none4noThe synthesis of a series of new chiral alpha-aminonitriles was achieved in a diastereoselect...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...
A simple and novel chiral amide-based organocatalyst <b>6</b> was synthesized from readily available...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
An organocatalytic enantioselective Strecker reaction for the synthesis of 3-amino-3-cyanooxindoles ...
Gröger H, Asano Y. Cyanide-Free Enantioselective Catalytic Strategies for the Synthesis of Chiral Ni...
The first organocatalytic asymmetric three-component Strecker reaction, the urea-catalyzed acylcyana...
Enantioselective synthesis of α-perfluoroalkylated cyclic amino acids and their derivatives was elab...
In summary, this work deals with the enantioselective synthesis of - and -amino nitriles, which can ...
A series of α-quaternary arylglycines were prepared in high optical purity (up to 98% ee) by α-alkyl...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
International audienceOptically active .alpha.-amino nitriles and .alpha.-amino phosphinic derivs. h...
A simple, convenient, and practical method for the synthesis of alpha-amino nitriles through a one-p...