A general and efficient synthesis of pyridin-2-yl C-ribonucleosides bearing diverse alkyl, aryl, amino, and carbamoyl groups in position 6

Journal of Organic Chemistry

Volumn 75, Issue 2, 2010, Pages 442-449

  Štefko, Martin ^a   Slavětínská, Lenka ^a   Klepetářová, Blanka ^a   Hocek, Michal ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMOYL GROUPS; CHEMICAL EQUATIONS; CROSS COUPLING REACTIONS; DEPROTECTION; EFFICIENT SYNTHESIS; HIGH YIELD; ONE POT; RIBOFURANOSE; RIBONUCLEOSIDES; TERT-BUTYLDIMETHYLSILYL;

ACETYLATION; ALKYLATION; CHEMICAL BONDS; PALLADIUM; REACTION INTERMEDIATES; SYNTHESIS (CHEMICAL);

AMINATION;

1BETA (6 BROMOPYRIDIN 2 YL) 1 O ACETYL 2,3,5 TRI O (TERT BUTYLDIMETHYLSILYL) DEXTRO RIBOFURANOSE; 2 LITHIO 6 BROMOPYRIDINE; ALCOHOL; ALKYL GROUP; AMINE; LITHIUM DERIVATIVE; PALLADIUM; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PYRIDIN 2 YL C RIBONUCLEOSIDE DERIVATIVE; PYRIDINE DERIVATIVE; RIBONUCLEOSIDE DERIVATIVE; UNCLASSIFIED DRUG;

ACETYLATION; AMINATION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS;

ALKANES; CARBAMATES; CATALYSIS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; MONOSACCHARIDES; PALLADIUM; RIBONUCLEOTIDES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 75349085720     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo902313g     Document Type: Article

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