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Synthesis of 4'-C-modified 2'-Deoxyribonucleoside Analogues and Oligonucleotides

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2008

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http://nbn-resolving.de/urn:nbn:de:bsz:352-opus-117538
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https://doi.org/10.2174/138527208783743705
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Current Organic Chemistry. 2008, 12(5), pp. 343-354. ISSN 1385-2728. eISSN 1875-5348. Available under: doi: 10.2174/138527208783743705

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4'-C-Modified nucleotides and oligonucleotides have been explored extensively recently. The motivations for these investigations drive from the development of new drugs to investigations of complex biological processes. This review covers the common strategies for the synthesis of 4'-C-modified nucleosides that have been subsequently incorporated into oligonucleotides. After a brief depiction of two mainly followed routes for the generation of 4'-C-modified nucleosides, the synthetic efforts of the modified nucleotides are grouped into those bearing hydrophobic or polar modifications. Subsequently strategies for the incorporation of the respective nucleotides into oligonucleotides by automated DNA synthesis are discussed.

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ISO 690MARX, Andreas, Karl-Heinz JUNG, 2008. Synthesis of 4'-C-modified 2'-Deoxyribonucleoside Analogues and Oligonucleotides. In: Current Organic Chemistry. 2008, 12(5), pp. 343-354. ISSN 1385-2728. eISSN 1875-5348. Available under: doi: 10.2174/138527208783743705
BibTex
@article{Marx2008Synth-3311,
  year={2008},
  doi={10.2174/138527208783743705},
  title={Synthesis of 4'-C-modified 2'-Deoxyribonucleoside Analogues and Oligonucleotides},
  number={5},
  volume={12},
  issn={1385-2728},
  journal={Current Organic Chemistry},
  pages={343--354},
  author={Marx, Andreas and Jung, Karl-Heinz}
}
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