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Tetrahedron

Volumn 67, Issue 30, 2011, Pages 5487-5493

Efficient synthesis of nucleoside aryloxy phosphoramidate prodrugs utilizing benzyloxycarbonyl protection

(4) Cho, Jong Hyun a Amblard, Franck a Coats, Steven J b Schinazi, Raymond F a

a EMORY UNIVERSITY SCHOOL OF MEDICINE (United States)

b RFS Pharma LLC (United States)

Author keywords

Antiviral; Benzyloxycarbonyl; Monophosphate prodrug; Nucleoside; ProTide

Indexed keywords

5' O [PHENYL (ETHOXYALANINYL)]PHOSPHORYL 2' FLUORO 2' METHYLCYTIDINE; 5' O [PHENYL (ETHOXYALANINYL)]PHOSPHORYL 2' FLUORO 2' METHYLURIDINE; 5' O [PHENYL (ETHOXYALANINYL)]PHOSPHORYLADENOSINE; 5' O [PHENYL (ETHOXYALANINYL)]PHOSPHORYLCYTIDINE; 5' O [PHENYL (ETHOXYALANINYL)]PHOSPHORYLGUANOSINE; 5' O [PHENYL (ETHOXYALANINYL)]PHOSPHORYLURIDINE; BENZYLOXYCARBONYL; CARBONYL DERIVATIVE; NUCLEOSIDE DERIVATIVE; PHOSPHATE; PRODRUG; UNCLASSIFIED DRUG;

ARTICLE; DEPROTECTION REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGENOLYSIS; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 79959333918 PISSN: 00404020 EISSN: 14645416 Source Type: Journal
DOI: 10.1016/j.tet.2011.05.046 Document Type: Article

Times cited : (19)

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