Olgodeoqnucleotides contarnug 4-thothymzdm residues were obtauwdusing the ph~?sphoramtdttes of 2 and J Treatment with CHJOSK tn EtOH was used to rntroduce the I-throketo $mctron at the olqodeoqnucleotrde level. Recently, we have reported the synthesis of 5'-0-(4,4'-dimethoxytrity1)-4-throcyanatothy
Solid-phase synthesis of oligodeoxynucleotides containing 4-alkoxythymidine residues
✍ Scribed by H. C. P. F. Roelen; H. F. Brugghe; H. van den Elst; G. A. van der Marel; J. H. van Boom
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 647 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Immobilized and fully protected oligodeoxynucleotides containing a 4‐(1,2,4‐triazolyl)‐thymidine residue at a predetermined position were prepared according to a well‐established phosphite triester methodology using 2‐cyanoethyl phosphoramidites of a 4‐(1,2,4‐triazolyl)‐substituted thymidine and standard protected nucleosides. Treatment of the immobilized oligomer with methanol, ethanol or n‐propanol in the presence of DBU at 50°C gave the corresponding oligonucleotides containing 4‐methoxy, 4‐ethoxy‐ or 4‐n‐propoxythymidine residue.
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