|
|
Volumn 67, Issue 8, 2002, Pages 2402-2410
|
|
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 β-amino acids
a,b
b
b
a
|
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
ROOM TEMPERATURE;
AMINO ACIDS;
CATALYSIS;
OLEFINS;
SYNTHESIS (CHEMICAL);
ESTERS;
ALKENE;
BETA AMINO ACID;
CYCLOBUTANE;
ESTER DERIVATIVE;
GLYCERALDEHYDE;
HYDROXYLAMINE;
OXAZOLIDINONE DERIVATIVE;
VERBENONE;
ARTICLE;
CALCULATION;
CATALYSIS;
CHIRALITY;
CYCLOADDITION;
ENANTIOMER;
LOW TEMPERATURE;
REACTION ANALYSIS;
ROOM TEMPERATURE;
STEREOCHEMISTRY;
SYNTHESIS;
THEORETICAL MODEL;
ALKANES;
AMINO ACIDS;
CATALYSIS;
CHEMISTRY, ORGANIC;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CRYSTALLOGRAPHY, X-RAY;
CYCLIZATION;
CYCLOBUTANES;
ESTERS;
GLYCERALDEHYDE;
HYDROXYLAMINES;
MAGNETIC RESONANCE SPECTROSCOPY;
MOLECULAR STRUCTURE;
STEREOISOMERISM;
TEMPERATURE;
TERPENES;
|
|
EID: 0037134171
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo0159082 Document Type: Article |
|
Times cited : (48)
|
|
References (34)
|
