The Strecker and Bucherer-Berg reaction are the most important strategies and powerful tools for the synthesis of α-amino acids from a carbonyl compound and cyanide. This chapter is an overview of the great work reported during the last 10 years in these two complementing fields which are two crucial methods for the preparation of α-aminoacids. Several remarkable examples regarding asymmetric works, interesting final structures or benign approaches will be disclosed and commented.Peer Reviewe
Trabajo presentado en el 19th European Symposium of Organic Chemistry, celebrado en Lisboa del 12 al...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
The research presented in this thesis had the objective to use enzymes and transition metal catalyst...
The first organocatalytic asymmetric three-component Strecker reaction, the urea-catalyzed acylcyana...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
The Multi-Component Reaction (MCRs) is a method in which three or more reactants are reacted in sing...
Both the Strecker and Bucherer-Bergs reactions convert the norbornane keto ester methyl bicyclo[2.2....
The building block approach was identified as a useful alternative to the commonly used Bucherer- Be...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
This thesis deals with the development and application of new synthetic methodology in organic chemi...
The synthesis of C-glycosyl beta-amino acids by asymmetric Mannich-type three-component reactions is...
The first Borono-Strecker reaction has been developed to synthesize α-aminoboronates via a multicomp...
An organocatalytic enantioselective Strecker reaction for the synthesis of 3-amino-3-cyanooxindoles ...
Piperidines, including Asymmetric Strategies ” is divided into four chapters. Chapter I deals with n...
Efficient and stereoselective synthetic routes to enantiomerically pure (2R,3S)- and (2R,3S)-2-amino...
Trabajo presentado en el 19th European Symposium of Organic Chemistry, celebrado en Lisboa del 12 al...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
The research presented in this thesis had the objective to use enzymes and transition metal catalyst...
The first organocatalytic asymmetric three-component Strecker reaction, the urea-catalyzed acylcyana...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
The Multi-Component Reaction (MCRs) is a method in which three or more reactants are reacted in sing...
Both the Strecker and Bucherer-Bergs reactions convert the norbornane keto ester methyl bicyclo[2.2....
The building block approach was identified as a useful alternative to the commonly used Bucherer- Be...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
This thesis deals with the development and application of new synthetic methodology in organic chemi...
The synthesis of C-glycosyl beta-amino acids by asymmetric Mannich-type three-component reactions is...
The first Borono-Strecker reaction has been developed to synthesize α-aminoboronates via a multicomp...
An organocatalytic enantioselective Strecker reaction for the synthesis of 3-amino-3-cyanooxindoles ...
Piperidines, including Asymmetric Strategies ” is divided into four chapters. Chapter I deals with n...
Efficient and stereoselective synthetic routes to enantiomerically pure (2R,3S)- and (2R,3S)-2-amino...
Trabajo presentado en el 19th European Symposium of Organic Chemistry, celebrado en Lisboa del 12 al...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
The research presented in this thesis had the objective to use enzymes and transition metal catalyst...