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Volumn 343, Issue 12, 2008, Pages 2057-2066
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The Amadori rearrangement as key reaction for the synthesis of neoglycoconjugates
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Author keywords
Amadori rearrangement; Carbohydrate amino acid conjugate; Neoglycoconjugate; Protein modification
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Indexed keywords
ADDITION REACTIONS;
AMINATION;
AMINES;
AMINO ACIDS;
CARBOHYDRATES;
HEALTH;
MICROFLUIDICS;
ORGANIC ACIDS;
ALIPHATIC AMINES;
AMINO ACID DERIVATIVES;
ANOMERIC;
APPLIED (CO);
ELSEVIER (CO);
GLUCOFURANOSE;
GLYCOCONJUGATES;
ISOLATED YIELDS;
NEOGLYCOCONJUGATES;
REACTION CONDITIONS;
SYNTHESIS (OF CHIRAL IONIC LIQUIDS);
TRIPHOSGENE;
ORGANIC COMPOUNDS;
AMINE;
AMINO ACID DERIVATIVE;
CARBAMIC ACID DERIVATIVE;
GLYCOCONJUGATE;
HEPTOSE;
NEOGLYCOCONJUGATE DERIVATIVE;
SUGAR;
AMADORI REARRANGEMENT;
ARTICLE;
CHEMICAL STRUCTURE;
NUCLEAR MAGNETIC RESONANCE;
PRIORITY JOURNAL;
SYNTHESIS;
GLYCOCONJUGATES;
GULO;
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EID: 45049085072
PISSN: 00086215
EISSN: None
Source Type: Journal
DOI: 10.1016/j.carres.2008.02.022 Document Type: Article |
Times cited : (28)
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References (48)
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