Convenient synthesis of 2′-deoxy-2-fluoroadenosine from 2-fluoroadenine

Nucleosides, Nucleotides and Nucleic Acids

Volumn 22, Issue 10, 2003, Pages 1899-1905

  Ye, Song ^a   Rezende, Martha M ^a   Deng, Wei Ping ^a   Kirk, Kenneth L ^a  

^a NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

Author keywords

Anomer separation; Fluorinated nucleosides; Glycosylation; Thioglycoside coupling

Indexed keywords

2 FLUORO 2' DEOXYADENOSINE DERIVATIVE; 2 FLUOROADENINE; 2' DEOXY 2 FLUOROADENOSINE; ADENINE DERIVATIVE; ADENOSINE DERIVATIVE; FLUORINE DERIVATIVE; FURAN DERIVATIVE; PHENYL 3,5 BIS[O (TERT BUTYLDIMETHYLSILYL)] 2 DEOXY 1 THIO DEXTRO ERYTHRO PENTOFURANOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHIRALITY; CHROMATOGRAPHY; DRUG STRUCTURE; DRUG SYNTHESIS; GLYCOSYLATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SILYLATION;

ADENINE; DEOXYADENOSINES; MOLECULAR STRUCTURE;

EID: 0142043373     PISSN: 15257770     EISSN: None     Source Type: Journal    
DOI: 10.1081/NCN-120025237     Document Type: Article

References (6)

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6. Ichikawa, Y.; Kubota, H.; Fujita, K.; Okauchi, T.; Narasaka, K. Stereoselective β-C and β-S-glycosylation of 2-deoxyribofuranose derivatives controlled by the 3-hydroxy protective group. Bull. Chem. Soc. Jpn. 1989, 62, 845-852.