A facile synthetic method for 3′-α-fluoro-2′,3′ -dideoxyadenosine

Nucleosides, Nucleotides and Nucleic Acids

Volumn 22, Issue 5-8, 2003, Pages 711-713

  Takamatsu, Satoshi ^a   Katayama, Satoshi ^a   Naito, Masaki ^a   Yamashita, Keizo ^a   Ineyama, Takashi ^a   Izawa, Kunisuke ^a  

^a AJINOMOTO CO INC   (Japan)

Author keywords

Anti HIV; Nucleosides Fluorination; Rearrangement

Indexed keywords

3' ALPHA FLUORO 2',3' DIDEOXYADENOSINE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; UNCLASSIFIED DRUG;

CONFERENCE PAPER; DRUG STRUCTURE; DRUG SYNTHESIS; FLUORINATION; REACTION ANALYSIS; STRUCTURE ACTIVITY RELATION;

ANTI-HIV AGENTS; DIDEOXYADENOSINE; INDICATORS AND REAGENTS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM;

HUMAN IMMUNODEFICIENCY VIRUS;

EID: 0141760401     PISSN: 15257770     EISSN: None     Source Type: Journal    
DOI: 10.1081/NCN-120022616     Document Type: Conference Paper

References (5)

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5. Takamatsu, S.; Katayama, S.; Hirose, N.; Naito, M.; Izawa, K. Tetrahedron Lett. 2001, 42, 7605-7608.