Phosphoramidite used to incorporate a deoxyuridine base into an oligonucleotide.
Phosphoramidite used to incorporate an iodo-modified deoxyuridine internally or at the 5' end of an oligonucleotide.
Phosphoramidite used to incorporate a fluoro-modified deoxyuridine internally or at the 5' end of an oligonucleotide.
Phosphoramidite used to incorporate a bromo-modified uridine internally or at the 5' end of an oligonucleotide.
This convertible nucleoside allows the formation of N4-alkyl-5-fluoro-dC residues by reaction with an alkyl amine.
Small, fluorescent natural base mimic that can signal the presence of abasic sites in hybridized DNA oligonucleotides.
Phosphoramidite for incorporation of a 4-thio-modified deoxyuridine in a synthetic oligonucleotide.
Modified nucleoside synthon.
Allows the introduction of a 5-aminoallyl-deoxyuridine residue into oligonucleotides for the purpose of post-synthetic labeling by acylation.
Phosphoramidite used to incorporate a 5-hydroxy-modified deoxyuridine into an oligonucleotide for epigenetic studies.
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