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