Chemical synthesis of 13C labeled anti-HIV nucleosides as mass-internal standards

Tetrahedron

Volumn 58, Issue 47, 2002, Pages 9593-9603

  Saito, Yoshio ^a   Zevaco, Thomas A ^b   Agrofoglio, Luigi A ^a  

^a UNIVERSITÉ D'ORLÉANS   (France)

^b KARLSRUHE INSTITUTE OF TECHNOLOGY   (Germany)

Author keywords

HIV; Labeled; Nucleosides

Indexed keywords

1 (2 O ACETYL 3,5 DI O BENZOYL BETA DEXTRO RIBOFURANOSYL) 5 METHYLURACIL C 13; 1 (2 O ACETYL 3,5 DI O BENZOYL BETA DEXTRO RIBOFURANOSYL)ADENINE C 13; 1 (2 O ACETYL 3,5 DI O BENZOYL BETA DEXTRO RIBOFURANOSYL)HYPOXANTHINE C 13; ANTIVIRUS AGENT; CARBOHYDRATE DERIVATIVE; DEXTRO 2',3' DIDEHYDRO 2',3' DIDEOXYTHYMIDINE C 13; DEXTRO 2',3' DIDEOXYADENOSINE C 13; DEXTRO 2',3' DIDEOXYINOSINE C 13; DEXTRO 2',3' O THIOCARBONYLENE 5' O TERT BUTYLDIMETHYLSILYLADENOSINE C 13; DEXTRO 2',3' O THIOCARBONYLENE 5' O TERT BUTYLDIMETHYLSILYLINOSINE C 13; DEXTRO 5 METHYL 2',3' O THIOCARBONYLENE 5' O TERT BUTYLDIMETHYLSILYLURIDINE C 13; NUCLEOSIDE DERIVATIVE; PERIODIC ACID; SODIUM BOROHYDRIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; COREY WINTER REACTION; COST BENEFIT ANALYSIS; DRUG SYNTHESIS; OXYGENATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION OPTIMIZATION; STANDARD; STEREOCHEMISTRY; VORBUGGEN REACTION;

EID: 0037131951     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)01246-2     Document Type: Article

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