|
Volumn 340, Issue 12, 2005, Pages 2039-2047
|
Synthesis and conformational studies on methyl 4-O-acetyl-3-azido-2,3,6- trideoxy-hex-5-enopyranosides of the L series
|
Author keywords
Anomeric effect; Enantiomers; Equatorial or axial orientation; Hex 5 enopyranosides; Iodination; Tosylation
|
Indexed keywords
IODINE;
METHANE;
NUCLEAR MAGNETIC RESONANCE;
SYNTHESIS (CHEMICAL);
GLYCOSIDES;
HYDROGEN IODIDE;
CONFORMATIONS;
PYRANOSIDE;
SULFONE DERIVATIVE;
ARTICLE;
CARBOHYDRATE ANALYSIS;
CARBOHYDRATE SYNTHESIS;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL MODIFICATION;
CONFORMATION;
ENERGY;
IODINATION;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
QUANTUM YIELD;
ACETYLATION;
AZIDES;
CARBOHYDRATE CONFORMATION;
DEOXY SUGARS;
NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR;
TOSYL COMPOUNDS;
|
EID: 22744452816
PISSN: 00086215
EISSN: None
Source Type: Journal
DOI: 10.1016/j.carres.2005.06.019 Document Type: Article |
Times cited : (2)
|
References (40)
|