Carbohydrate scaffolds for combinatorial syntheses that allow selective deprotection of all four positions independent of the sequence

Angewandte Chemie - International Edition

Volumn 43, Issue 9, 2004, Pages 1104-1107

  Hünger, Udo ^a   Ohnsmann, Janina ^a   Kunz, Horst ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

Carbohydrates; Combinatorial chemistry; Orthogonal protecting groups; Protecting groups; Solid phase synthesis

Indexed keywords

AMINO ACIDS; MOLECULES; SCAFFOLDS; SYNTHESIS (CHEMICAL);

COMBINATORIAL DIVERSIFICATION; FUNCTIONAL GROUPS; PEPTIDES; SIDE CHAINS;

CARBOHYDRATES;

AMINO ACID; CARBOHYDRATE; PEPTIDE;

AMINO ACID SEQUENCE; ARTICLE; CARBOHYDRATE ANALYSIS; COMBINATORIAL CHEMISTRY; DEPROTECTION REACTION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SOLID; STRUCTURE ANALYSIS; SYNTHESIS;

CARBOHYDRATES; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COMBINATORIAL CHEMISTRY TECHNIQUES; DRUG DESIGN; GLYCOSIDES; MASS SPECTROMETRY; MOLECULAR STRUCTURE; STEREOISOMERISM; THIOGLYCOSIDES;

EID: 4544262327     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200352919     Document Type: Article

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