Synthesis of 6-aryl-2′-deoxyuridine nucleosides via a Liebeskind cross-coupling methodology

Tetrahedron Letters

Volumn 53, Issue 2, 2012, Pages 253-255

  Kögler, Martin ^a   De Jonghe, Steven ^a   Herdewijn, Piet ^a  

^a REGA INSTITUTE FOR MEDICAL RESEARCH   (Belgium)

Author keywords

6 Substituted 2 deoxyuridine nucleoside analogues; Copper thiophene carboxylate; Liebeskind cross coupling reaction

Indexed keywords

6 (4 FLUOROPHENYL) 2' DEOXYURIDINE 5' MONOPHOSPHATE; BORONIC ACID DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; COPPER THIOPHENE CARBOXYLIC ACID; DEOXYURIDINE DERIVATIVE; ESTER; FLUORIDE; GLYCOSIDE; NUCLEOSIDE ANALOG; NUCLEOTIDE DERIVATIVE; PALLADIUM; REAGENT; UNCLASSIFIED DRUG;

ALKALINITY; ARTICLE; CATALYSIS; CHEMICAL BOND; CROSS COUPLING REACTION; DESILYLATION; DRUG SYNTHESIS; LIEBESKIND CROSS COUPLING REACTION; MOLECULAR STABILITY; PHOSPHORYLATION; STOICHIOMETRY; SUZUKI REACTION; TEMPERATURE; YOSHIKAWA PHOSPHORYLATION;

EID: 83555178378     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.11.036     Document Type: Article

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