Convertible nucleoside phosphoramidite that allows the formation of N4-alkyl-C residues in RNA for structural studies.
Phosphoramidite used to incorporate a 5-hydroxy-modified deoxycytidine into an oligonucleotide for epigenetic studies.
Phosphoramidite used to incorporate a 2’-O-methoxyethyl-modified methyl-U into an oligonucleotide, useful for antisense RNA.
Des-methyl analog of cytidine useful for probing the hydrogen-bonding characterisitcs in oligonucleotides.
Phosphoramidite used to incorporate a BlackBerry-650™ moiety either internally or at the 5' end of an oligonucleotide.
Phosphoramidite for incorporation of a 6-thio-modified guanosine in a synthetic oligonucleotide.
Phenoxyacetyl (Pac) protected 2'-OTBDMS phosphoramidite for the incorporation of ribo-A into a synthetic oligonucleotide using UltraMILD conditions.
Phosphoramidite for incorporation of cholesterol internally or at 5' end of an oligonucleotide, with a triethylene glycol spacer.
Half of a novel base pair (with d5SICS) that achieves pair recognition through hydrophobic interactions.
UltraMILD phenoxyacetyl (Pac) monomers are designed to withstand prolonged exposure to strongly alkaline conditions during heating with ammonium hydroxide solution.
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