A general regioselective approach to 2,4-disubstituted pyrimidin-5-yl C-2-deoxyribonucleosides

Synthesis

Volumn 44, Issue 6, 2012, Pages 953-965

  Kubelka, Tomá ^a   Slavtínská, Lenka ^a   Hocek, Michal ^a,b  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

^b CHARLES UNIVERSITY   (Czech Republic)

Author keywords

cross coupling; Heck reaction; nucleophilic aromatic substitution; nucleosides; regioselectivity

Indexed keywords

C-NUCLEOSIDES; CROSS COUPLING REACTIONS; CROSS-COUPLINGS; DESILYLATION; DOUBLE SUBSTITUTION; ELEVATED TEMPERATURE; HECK COUPLING; HECK REACTIONS; MODULAR SYNTHESIS; NUCLEOPHILIC AROMATIC SUBSTITUTION; NUCLEOPHILIC SUBSTITUTIONS; NUCLEOSIDES; REGIO-SELECTIVE; REGIOSELECTIVE REACTIONS;

CHEMISTRY; SPEECH SYNTHESIS;

REGIOSELECTIVITY;

2,6 DICHLORO 5 IODOPYRIMIDINE; 2,6 DICHLOROPYRIMIDIN 5 YL; DEOXYRIBONUCLEOSIDE; GLYCAN; PYRIMIDINE DERIVATIVE; REAGENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REDUCTION; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; DESILYLATION; HIGH TEMPERATURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SUZUKI REACTION; SYNTHESIS; X RAY DIFFRACTION;

EID: 84858069497     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1289694     Document Type: Article

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