Nucleosides and nucleotides. 127. A novel and convenient post-synthetic modification method for the synthesis of oligodeoxyribonucleotides carrying amino linkers at the 5-position of 2′-deoxyuridine
- 20 January 1994
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 4 (2) , 361-366
- https://doi.org/10.1016/s0960-894x(01)80145-1
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- The synthesis of modified oligonucleotides by the phosphoramidite approach and their applicationsTetrahedron, 1993
- The Functionalization of Oligonucleotides Via Phosphoramidite DerivativesTetrahedron, 1993
- 6-O-(Pentafluorophenyl)-2'-deoxyguanosine: a versatile synthon for nucleoside and oligonucleotide synthesisThe Journal of Organic Chemistry, 1992
- A postoligomerization synthesis of oligodeoxynucleotides containing polycyclic aromatic hydrocarbon adducts at the N6 position of deoxyadenosine.Journal of the American Chemical Society, 1992
- Advances in the Synthesis of Oligonucleotides by the Phosphoramidite ApproachTetrahedron, 1992
- Synthesis by post-synthetic substitution of oligomers containing guanine modified at the 6-position with S-, N-, O-derivativesTetrahedron, 1992
- Disulfide-crosslinked oligonucleotidesJournal of the American Chemical Society, 1991
- Engineering tethered DNA molecules by the convertible nucleoside approachTetrahedron, 1991
- Synthesis of functionally tethered oligodeoxynucleotides by the convertible nucleoside approachThe Journal of Organic Chemistry, 1990
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesisTetrahedron Letters, 1981