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.
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.
Phosphoramidite useful for synthesising 2'-5' linked oligonucleotides.
Phosphoramidite for the incorporation of a carboxylate function either internally or at the 5' end of an oligonucloetide, with a dT nucleobase.
A stable phosphoramidite analogue of N3-methyladenine (3-Me-A).
Phosphoramidite for incorporation of a C12 spacer internally or at the 5' end of an oligonucleotide.
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