A stereoselective synthesis of (5′ S)‐5′‐C‐(5‐bromo‐2‐penten‐1‐yl)‐2′‐
deoxyribofuranosyl thymine phosphoramidite is described; the absolute stereochemistry of …

We describe the preparation and fluorescence properties of a set of new nucleosides in
which a known hydrocarbon or oligothiophene fluorophore replaces the DNA base at C (1) …

1-(2, 3-Dideoxy-3-amino-α-d-arabino-hexofuranosyl) thymine is considered as a
conformationally restricted acyclic nucleoside using the furanose ring to link the diol …

Convergent synthesis of β-and α-1-(3-C-allyl-2-deoxy-D-erythro-pentofuranosyl) thymine
and their incorporation into β-and α-oligodeoxynucleotides (ODNs) is described. The …

Post-synthetic functionalization of oligodeoxyribonucleotides at the 2′-position - ScienceDirect Skip
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An achiral, acyclic nucleoside analogue has been incorporated once or twice in
oligodeoxyribonucleotides by the phosphoramidite method, and conditions found which …

Oligonucleotides containing 5-hydroxy-2′-deoxycytidine (2) have been synthesized using
the phosphoramidite chemistry. The presence and the integrity of the modified nucleoside in …

Novel 5'-C-hydroxymethyl substituted derivatives of thymidine have been prepared by
dihydroxylation of the 5'-C-methylene nucleoside 1. Osmium tetraoxide catalysed …

Abstract We synthesized 3′-O-dimethoxytrityl-5′ O-phosphoramidites and 5′-O-
succinates which can be used as monomeric building blocks for the built up of …

Novel Oligodeoxynucleotide analogues containing 3′-C-threo-methylene phosphodiester
internucleoside linkages were synthesized on automated DNA-synthesizers using the …