The first organocatalytic asymmetric three-component Strecker reaction, the urea-catalyzed acylcyanation of in situ generated imines, has been developed. Different α-amido nitriles are formed in excellent yields and enantioslectivities from aldehydes, amines, and acyl cyanides in the presence of Jacobsen's thiourea catalyst 5. Despite its obvious use for the synthesis of α-amino acids and their derivatives, our reaction may find use in diversity oriented synthesis and medicinal chemistry
none4noThe synthesis of a series of new chiral alpha-aminonitriles was achieved in a diastereoselect...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...
A convenient and efficient one-pot method for the synthesis of a variety of α-amino nitriles from al...
The catalytic acylcyanation of aldimines with acylcyanides and a direct three‐component variant invo...
Different aldehydes and amines react with acyl cyanides in the presence of a catalytic amount of the...
An organocatalytic enantioselective Strecker reaction for the synthesis of 3-amino-3-cyanooxindoles ...
A simple and novel chiral amide-based organocatalyst <b>6</b> was synthesized from readily available...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
Axially chiral N,N'-dioxide Lewis base promoters have been developed and have for the first time bee...
The Strecker and Bucherer-Berg reaction are the most important strategies and powerful tools for the...
The asymmetric Strecker reaction of aldimines and trimethylsilyl cyanide promoted by 1 equivalent of...
Aldimines react with acetyl cyanide in the presence of a catalytic amount of a thiourea catalyst to ...
A simple, convenient, and practical method for the synthesis of alpha-amino nitriles through a one-p...
none4noThe synthesis of a series of new chiral alpha-aminonitriles was achieved in a diastereoselect...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...
A convenient and efficient one-pot method for the synthesis of a variety of α-amino nitriles from al...
The catalytic acylcyanation of aldimines with acylcyanides and a direct three‐component variant invo...
Different aldehydes and amines react with acyl cyanides in the presence of a catalytic amount of the...
An organocatalytic enantioselective Strecker reaction for the synthesis of 3-amino-3-cyanooxindoles ...
A simple and novel chiral amide-based organocatalyst <b>6</b> was synthesized from readily available...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
Axially chiral N,N'-dioxide Lewis base promoters have been developed and have for the first time bee...
The Strecker and Bucherer-Berg reaction are the most important strategies and powerful tools for the...
The asymmetric Strecker reaction of aldimines and trimethylsilyl cyanide promoted by 1 equivalent of...
Aldimines react with acetyl cyanide in the presence of a catalytic amount of a thiourea catalyst to ...
A simple, convenient, and practical method for the synthesis of alpha-amino nitriles through a one-p...
none4noThe synthesis of a series of new chiral alpha-aminonitriles was achieved in a diastereoselect...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...
A convenient and efficient one-pot method for the synthesis of a variety of α-amino nitriles from al...