Electrochemistry of chalcogenoglycosides. Rational design of iterative glycosylation based on reactivity control of glycosyl donors and acceptors by oxidation potentials

Journal of Organic Chemistry

Volumn 67, Issue 24, 2002, Pages 8584-8592

  Yamago, Shigeru ^a   Kokubo, Koji ^a   Hara, Osamu ^a   Masuda, Sadayoshi ^a   Yoshida, Jun ichi ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSYLATION;

ELECTROLYSIS; ORGANIC COMPOUNDS; OXIDATION; SUBSTITUTION REACTIONS;

ELECTROCHEMISTRY;

CHALCOGEN; CHALCOGENOGLYCOSIDE; GLYCOSIDE; OLIGOSACCHARIDE; PHENYLSELENOGLUCOPYRANOSIE; PHENYLTELLUROGLUCOPYRANOSIDE; PHENYLTHIOGLUCOPYRANOSIDE; UNCLASSIFIED DRUG; SELENIUM;

AB INITIO CALCULATION; ARTICLE; CALCULATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; DECOMPOSITION; ELECTROCHEMISTRY; ELECTROLYSIS; ENERGY; GLYCOSYLATION; IONIZATION; OXIDATION REDUCTION POTENTIAL; POTENTIOMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; CHEMISTRY; COMBINATORIAL CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM;

CHALCOGENS; COMBINATORIAL CHEMISTRY TECHNIQUES; ELECTROCHEMISTRY; GLYCOSIDES; GLYCOSYLATION; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; SELENIUM; STEREOISOMERISM;

EID: 0037195684     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0261350     Document Type: Article

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