Used for oligo synthesis in the reverse direction.
Modified nucleoside synthon.
Modified nucleoside synthon.
Useful addtion to the nebularine family for hydrogen bonding studies.
Phosphoramidite used to replace thymidine residues in oligonucleotides, for duplex stabilization.
The C-nucleoside 2'-deoxypseudouridine, in contrast to dU, forms stable C:pseudoU-A triplets.
A state-of-the-art cyclooctyne for catalyst free strain-promoted, copper-free azide-alkyne cycloadditions.
Phosphoramidite to incorporate an amino functionality on deoxyuridine, for post-synthetic conjugation.
A C-nucleoside phosphoramidite that is isosteric with deoxycytidine and has additional hydrogen-bonding ability.
Phosphoramidite used to incorporate a 8-amino-modified deoxyadenosine into an oligonucleotide.
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