
Tetrahedron Letters p. 6649 - 6652 (1994)
Update date:2022-08-04
Topics:
Quant, S.
Wechselberger, R. W.
Wolter, M. A.
Woerner, K.-H.
Schell, P.
et al.
The preparation of 13C-labelled ribonucleosides starting from <13C6>-glucose 1 and the corresponding nucleobases 5a-e or 6a-e (N6-benzoyl-adenine, N2-acetyl-guanine, N4-benzoyl-cytosine, uracil and thymine) in 47-66percent overall yield is described.Their subsequent transformation into 5'-O-dimethoxytrityl protected DNA-phosphoramidites and 5'-O-dimethoxytrityl-2'-O-trialkylsilyl protected RNA-phosphor-amidites for the solid phase synthesis of DNA- and RNA-oligomers and to 5'-O-ribo- and deoxyribo-nucleosidetriphosphates for template controlled enzymatic synthesis (polymerase- or reverse transcriptase reaction) has been carried out.
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