Triplex formation by an oligonucleotide containing conformationally locked C-nucleoside, 5-(2-O,4-C-methylene-β-d-ribofuranosyl)oxazole
- 1 January 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (2) , 221-224
- https://doi.org/10.1016/s0040-4039(99)02052-3
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Synthesis of conformationally locked C-nucleosides having a 2,5-dioxabicyclo[2.2.1]heptane ring systemTetrahedron Letters, 2000
- Synthesis and Thermodynamic and Biophysical Properties of Tricyclo-DNAJournal of the American Chemical Society, 1999
- Hybridization properties of base-modified oligonucleotides within the double and triple helix motifEuropean Journal of Medicinal Chemistry, 1998
- Triplex formation by oligonucleotides containing novel deoxycytidine derivatives [published erratum appears in Nucleic Acids Res 1997 Sep 15;25(18):following 3750]Nucleic Acids Research, 1996
- Sequence‐Specific Recognition and Modification of Double‐Helical DNA by OligonucleotidesAngewandte Chemie International Edition in English, 1993
- Recognition of all four base pairs of double-helical DNA by triple-helix formation: design of nonnatural deoxyribonucleosides for pyrimidine.cntdot.purine base pair bindingJournal of the American Chemical Society, 1992
- Effects of an abasic site on triple helix formation characterized by affinity cleavingNucleic Acids Research, 1991