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Synthesis of nucleoside 5'-S-methylphosphonates and related compounds
I. Kósíová, I. Rosenberg,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18776507
DOI
10.1093/nass/nrn288
Knihovny.cz E-zdroje
- MeSH
- kyseliny fosforité chemická syntéza chemie MeSH
- nukleotidy chemická syntéza chemie MeSH
- oligonukleotidy chemická syntéza MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Phosphonate analogs of mono- and oligonucleotides with the P-C-O-C5' moiety have interesting biochemical and biophysical properties. A series of novel compounds, S-methylphosphonate-based nucleotides, with the P-C-S-C5' linkage was prepared as monomers for solid phase synthesis of modified oligonucleotides. Replacement of the 5'-oxygen atom with more nucleophilic, bulky, and lipophilic sulfur atom may influence the physicochemical and biological properties of nucleoside 5'-S-methylphosphonates and chimeric oligonucleotides as well.
Citace poskytuje Crossref.org
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