Convertible phosphoramidite that allows the formation of N6-alkyl-dA residues through reaction with alkyl amines.
This phosphoramidite allows incorporation of an etheno bridged dG moiety internally or at the 5’ end of an oligonucleotide.
Allows the introduction of a 5-aminoallyl-deoxyuridine residue into oligonucleotides for the purpose of post-synthetic labeling by acylation.
Phosphoramidite used to incorporate an amino-modified dT into an oligonucleotide, with a 15-atom spacer.
Phosphoramidite for the incorporation of a 2-thiodeoxythymidine modification into oligonucleotides.
Modified nucleoside synthon.
Useful phosphoramidite for modification of base pairing and metal chelating characterisitcs of purine nucleosides through elimination of the N7 nitrogen.
Phosphoramidite used to incorporate a chloro-modified deoxycytidine internally or at the 5' end of an oligonucleotide.
Phosphoramidite used to incorporate a 5-hydroxymethyl-modified deoxycytidine into an oligonucleotide for epigenetic studies.
Phosphoramidite used to incorporate metal-chelating functionality into an oligonucleotide.
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