Ritter-type reaction of C-(1-bromo-1-deoxy-d-glycopyranosyl)formamides and its application for the synthesis of oligopeptides incorporating anomeric α-amino acids

Carbohydrate Research

Volumn 346, Issue 14, 2011, Pages 2104-2112

  Czifrák, Katalin ^a   Gyóllai, Viktor ^a   Kövér, Katalin E ^a   Somsák, László ^a  

^a UNIVERSITY OF DEBRECEN   (Hungary)

Author keywords

2 Amino 2 deoxy hept(hex) 2 ulopyranosononitrile; 2 Bromo 2 deoxy hept(hex) 2 ulopyranosonamide; Anomeric amino acid; Oligopeptide; Ritter reaction

Indexed keywords

2-AMINO-2-DEOXY-HEPT(HEX)-2-ULOPYRANOSONONITRILE; 2-BROMO-2-DEOXY-HEPT(HEX)-2-ULOPYRANOSONAMIDE; ANOMERICS; OLIGOPEPTIDE; RITTER-REACTION;

AMINO ACIDS; CYANIDES; ORGANIC POLYMERS; SILVER COMPOUNDS;

SYNTHESIS (CHEMICAL);

ALPHA AMINO ACID; AMINOSUGAR; C (1 BROMO 1 DEOXY DEXTRO GLYCOPYRANOSYL)FORMAMIDE DERIVATIVE; DIPEPTIDE; FORMAMIDE DERIVATIVE; GROUPS WITH A CARBON-NITROGEN BOND ONLY; INDIUM CHLORIDE; MERCURIC OXIDE; MERCURIC OXYCYANIDE; NITRILE; OLIGOPEPTIDE; OXAZOLINE DERIVATIVE; SILVER; TRIPEPTIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBOHYDRATE SYNTHESIS; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; HYDROLYSIS; PRIORITY JOURNAL; RITTER REACTION;

AMINO ACIDS; FORMAMIDES; OLIGOPEPTIDES; STEREOISOMERISM;

TETRA;

EID: 80052766869     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2011.07.001     Document Type: Article

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