Reaction between N-alkylhydroxylamines and chiral enoate esters: more experimental evidence for a cycloaddition-like process, a rationale based on DFT theoretical calculations, and stereoselective synthesis of new enantiopure beta-amino acids.
Moglioni, Albertina G
Reaction between N-alkylhydroxylamines and chiral enoate esters: more experimental evidence for a cycloaddition-like process, a rationale based on DFT theoretical calculations, and stereoselective synthesis of new enantiopure beta-amino acids. [electronic resource] - The Journal of organic chemistry Apr 2002 - 2402-10 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0022-3263
10.1021/jo0159082 doi
Alkanes--chemistry
Amino Acids--chemical synthesis
Bicyclic Monoterpenes
Catalysis
Chemistry, Organic--methods
Chromatography, High Pressure Liquid
Crystallography, X-Ray
Cyclization
Cyclobutanes--chemistry
Esters--chemistry
Glyceraldehyde--chemistry
Hydroxylamines--chemistry
Magnetic Resonance Spectroscopy
Molecular Structure
Stereoisomerism
Temperature
Terpenes--chemistry
Reaction between N-alkylhydroxylamines and chiral enoate esters: more experimental evidence for a cycloaddition-like process, a rationale based on DFT theoretical calculations, and stereoselective synthesis of new enantiopure beta-amino acids. [electronic resource] - The Journal of organic chemistry Apr 2002 - 2402-10 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0022-3263
10.1021/jo0159082 doi
Alkanes--chemistry
Amino Acids--chemical synthesis
Bicyclic Monoterpenes
Catalysis
Chemistry, Organic--methods
Chromatography, High Pressure Liquid
Crystallography, X-Ray
Cyclization
Cyclobutanes--chemistry
Esters--chemistry
Glyceraldehyde--chemistry
Hydroxylamines--chemistry
Magnetic Resonance Spectroscopy
Molecular Structure
Stereoisomerism
Temperature
Terpenes--chemistry