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Volumn 65, Issue 26, 2000, Pages 8988-8996
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Synthesis of pyrimidine 2′-deoxy ribonucleosides branched at the 2′-position via radical atom-transfer cyclization reaction with a vinylsilyl group as a radical-acceptor tether
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Author keywords
[No Author keywords available]
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Indexed keywords
1 (2 DEOXY 2 C HYDROXYMETHYL BETA DEXTRO RIBOPENTOFURANOSYL)CYTOSINE;
1 (2 DEOXY 2 C HYDROXYMETHYL BETA DEXTRO RIBOPENTOFURANOSYL)URACIL;
1 (2 DEOXY 2 C VINYL BETA DEXTRO RIBOPENTOFURANOSYL)CYTOSINE;
1 (2 DEOXY 2 C VINYL BETA DEXTRO RIBOPENTOFURANOSYL)URACIL;
ANTINEOPLASTIC AGENT;
ANTIVIRUS AGENT;
BENZENE DERIVATIVE;
DEOXYCYTIDINE;
DEOXYRIBONUCLEOSIDE;
IMIDAZOLE;
METHYL GROUP;
PYRIMIDINE DERIVATIVE;
RADICAL;
REAGENT;
SILANE DERIVATIVE;
TETRABUTYLAMMONIUM;
UNCLASSIFIED DRUG;
VINYL DERIVATIVE;
ARTICLE;
CHEMICAL MODIFICATION;
CHEMICAL REACTION;
CYCLIZATION;
DRUG SYNTHESIS;
REACTION ANALYSIS;
REDUCTION;
STEREOCHEMISTRY;
ANTINEOPLASTIC AGENTS;
CYCLIZATION;
DEOXYRIBONUCLEOSIDES;
FREE RADICALS;
MAGNETIC RESONANCE SPECTROSCOPY;
STEREOISOMERISM;
VINYL COMPOUNDS;
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EID: 0034731577
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo000967l Document Type: Article |
Times cited : (29)
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References (65)
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