Abstract
A strategy was developed for the synthesis of 3'-O-beta-D-ribofuranosyl 2'-deoxythymidine derivatives using three different protecting groups, which allows the synthesis of a phosphoramidite building block for oligonucleotide synthesis. Likewise the 5'-O- and 5''-O-phosphorylated analogues were synthesized and their conformation was determined using NMR spectroscopy.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Magnetic Resonance Spectroscopy
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Mass Spectrometry
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Oligonucleotides / chemical synthesis*
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Oligonucleotides / chemistry*
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Organophosphorus Compounds / chemistry
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Phosphorylation
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Thymidine / chemical synthesis*
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Thymidine / chemistry*
Substances
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Oligonucleotides
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Organophosphorus Compounds
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phosphoramidite
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Thymidine