SCOPUS 정보 검색 플랫폼

Volumn 344, Issue 4, 2009, Pages 448-453

Synthesis of the first example of a nucleoside analogue bearing a 5′-deoxy-β-d-allo-septanose as a seven-membered ring sugar moiety

(9) Sizun, Gwenaëlle a Dukhan, David a Griffon, Jean François a Griffe, Ludovic a Meillon, Jean Christophe a Leroy, Frédéric a Storer, Richard a Sommadossi, Jean Pierre b Gosselin, Gilles a

a Idenix Pharmaceuticals (France)

b Idenix Pharmaceuticals Inc (United States)

Author keywords

Antiviral evaluation; Oxepane nucleosides; Septanose carbohydrates; Synthesis

Indexed keywords

ANTI-VIRAL EFFECTS; ANTIVIRAL EVALUATION; NUCLEOSIDE ANALOGUES; OXEPANE NUCLEOSIDES; SEPTANOSE CARBOHYDRATES; SEVEN-MEMBERED RINGS; SUGAR MOIETIES; SYNTHESIS;

BEARINGS (STRUCTURAL); CELL CULTURE; NUCLEOTIDES; ORGANIC COMPOUNDS; SUGAR (SUCROSE); SUGARS;

SYNTHESIS (CHEMICAL);

9 (5 DEOXY BETA DEXTRO ALLOSEPTANOSYL)ADENINE; HEPTOSE; LACTONE DERIVATIVE; NUCLEOSIDE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIVIRAL ACTIVITY; ARTICLE; CARBOHYDRATE SYNTHESIS; CONTROLLED STUDY; CYTOTOXICITY; DRUG SYNTHESIS; FLAVIVIRUS; NONHUMAN; PICORNAVIRUS; POXVIRUS; PRIORITY JOURNAL; RETROVIRUS;

ANTIVIRAL AGENTS; FLAVIVIRUS; HEPACIVIRUS; MODELS, CHEMICAL; MOLECULAR STRUCTURE; NUCLEOSIDES; OLIGOSACCHARIDES; PESTIVIRUS;

GULO;

EID: 61349166448 PISSN: 00086215 EISSN: None Source Type: Journal
DOI: 10.1016/j.carres.2008.12.019 Document Type: Article

Times cited : (13)

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