The C-nucleoside 2'-deoxypseudouridine, in contrast to dU, forms stable C:pseudoU-A triplets.
Classic 2'-OTBDMS phosphoramidite for incorporation of U into a synthetic oligonucleotide.
A state-of-the-art cyclooctyne for catalyst free strain-promoted, copper-free azide-alkyne cycloadditions.
Phosphoramidite for the efficient incorporation of a fluorescent deoxycytidine analogue into oligonucleotides.
Phosphoramidite for incorporation of a 2'-O-methyl modified ribo-C nucleobase within an oligonucleotide
Phosphoramidite used to incorporate a thiol functionality, with ether spacer, in an oligonucleotide.
Phosphoramidite used to incorporate a 5'-capped dT in an oligonucleotide.
Phosphoramidite for incorporation of an (otherwise unmodified) reverse (5’ to 3’) dT nucleobase within an oligonucleotide.
Phosphoramidite to incorporate an amino functionality on deoxyuridine, for post-synthetic conjugation.
Fluorous-tagged nucleoside useful for the purification of oligonucleotides.
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