A highly diastereoselective synthesis of α-hydroxy-β-amino acid derivatives via a Lewis acid catalyzed three-component condensation reaction.
Gassa, Federico
A highly diastereoselective synthesis of α-hydroxy-β-amino acid derivatives via a Lewis acid catalyzed three-component condensation reaction. [electronic resource] - The Journal of organic chemistry Nov 2010 - 7099-106 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1520-6904
10.1021/jo1011762 doi
Aldehydes--chemistry
Amines--chemistry
Amino Acids--chemical synthesis
Catalysis
Ethylenes--chemistry
Ketones--chemistry
Lewis Acids--chemistry
Models, Molecular
Molecular Conformation
Stereoisomerism
Substrate Specificity
A highly diastereoselective synthesis of α-hydroxy-β-amino acid derivatives via a Lewis acid catalyzed three-component condensation reaction. [electronic resource] - The Journal of organic chemistry Nov 2010 - 7099-106 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1520-6904
10.1021/jo1011762 doi
Aldehydes--chemistry
Amines--chemistry
Amino Acids--chemical synthesis
Catalysis
Ethylenes--chemistry
Ketones--chemistry
Lewis Acids--chemistry
Models, Molecular
Molecular Conformation
Stereoisomerism
Substrate Specificity