|
Volumn 124, Issue 29, 2002, Pages 8637-8643
|
Design and synthesis of a novel class of sugar-peptide hybrids: C-linked glyco β-amino acids through a stereoselective "acetate" Mannich reaction as the key strategic element
|
Author keywords
[No Author keywords available]
|
Indexed keywords
OXIDATIVE TREATMENT;
ALDEHYDES;
AMINO ACIDS;
DERIVATIVES;
HYDROLYSIS;
MOLECULAR DYNAMICS;
NUCLEAR MAGNETIC RESONANCE;
OLIGOMERS;
SYNTHESIS (CHEMICAL);
NITROGEN COMPOUNDS;
ACETIC ACID;
ALDEHYDE DERIVATIVE;
AMMONIUM DERIVATIVE;
BETA AMINO ACID;
CAMPHOR;
CARBONYL DERIVATIVE;
CERIUM NITRATE;
GLYCOSIDE;
ISOBORNEOL;
LITHIUM DERIVATIVE;
OLIGOMER;
OLIGOPEPTIDE;
PEPTIDE DERIVATIVE;
SUGAR;
SULFONE DERIVATIVE;
ARTICLE;
CHEMICAL MODIFICATION;
CHEMICAL REACTION;
CHIRALITY;
CONFORMATIONAL TRANSITION;
DIASTEREOISOMER;
HYBRID;
MANNICH REACTION;
MOLECULAR DYNAMICS;
PEPTIDE SYNTHESIS;
PROTEIN STRUCTURE;
REACTION ANALYSIS;
STEREOCHEMISTRY;
AMINO ACIDS;
CARBOHYDRATE CONFORMATION;
CRYSTALLOGRAPHY, X-RAY;
GLYCOPEPTIDES;
GLYCOSIDES;
HEXOSES;
MODELS, MOLECULAR;
NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR;
PROTEIN CONFORMATION;
STEREOISOMERISM;
SUBSTRATE SPECIFICITY;
|
EID: 0037167030
PISSN: 00027863
EISSN: None
Source Type: Journal
DOI: 10.1021/ja026250s Document Type: Article |
Times cited : (111)
|
References (119)
|