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]
Producer: 20020815Description: 2402-10 p. digitalISSN:- 0022-3263
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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