5′-5′ Tethered oligonucleotides via nucleic bases: a potential new set of compounds for alternate strand triple-helix formation

U Asseline, NT Thuong - Tetrahedron letters, 1994 - Elsevier
The solid-phase synthesis of 5′-5′-linked oligonucleotides tethered via nucleic bases and
with opposite polarities has been performed using a modified dinucleoside bearing a …

Oligonucleotides tethered via nucleic bases. A potential new set of compounds for alternate strand triple-helix formation

U Asseline, NT Thuong - Tetrahedron letters, 1993 - Elsevier
Oligonucleotides Tethered via Nucleic Bases. A Potential New Set of Compounds for Alternate
Strand Triple-Helix Formation Page 1 Tehahcdron Letters, Vol. 34. No. 26. pp. 41734176.1993 …

Synthesis of Triple Helix Forming Oligonucleotides with a Phenanthroline Moiety into the 3′‐3′ Inversion Site of Polarity

V Esposito, A Galeone, L Mayol… - European Journal of …, 2002 - Wiley Online Library
A protocol for the synthesis of triplex forming oligonucleotides containing a chelating
molecule in the 3′‐3′ inversion site of polarity is reported. A number of 16‐mers have …

A Facile Solid‐Phase Synthesis of Oligonucleotides Containing a 3′− 3′ Phosphodiester Bond for Alternate Strand Triple‐Helix Formation

L De Napoli, G Di Fabio, A Messere… - European journal of …, 1998 - Wiley Online Library
An improved protocol for the synthesis of oligonucleotides containing a 3′− 3′
phosphodiester linkage, for use in an alternate strand triple‐helix formation approach, is …

Deoxyoligonucleotides with Inverted Polarity Synthesis and Use in Triple-Helix Formation

S McCurdy, C Moulds, B Froehler - Nucleosides and Nucleotides, 1991 - Taylor & Francis
Deoxyoligonucleotides with Inverted Polarity Synthesis and Use in Triple-Helix Formation
Page 1 NUCLEOSIDES & NUCLEOTIDES, lO(1-3), 287-290 (1991) …

Facile preparation of 3′-derivatized oligodeoxynucleotides

A Peyman, C Weiser, E Uhlmann - Bioorganic & Medicinal Chemistry …, 1995 - Elsevier
We present a facile method for the preparation of 3′-derivatized oligonucleotides. It
involves the use of a universal solid support coupled linker molecule 1 carrying two …

Synthesis of 3′-functionalized oligonucleotides on a single solid support

J Hovinen, A Guzaev, A Azhayev, H Lönnberg - Tetrahedron Letters, 1993 - Elsevier
SYNTHESIS OF 3’-FUNCTIONALIZED OLIGONUCLEOTIDES ON A SINGLE SOLID SUPPORT
Page 1 Teuahcdnm Lanaa. Vol. 34. No. SO. pi 8169-8172 1993 Rited in Grca Britain …

Synthesis of 3 '-3 '-Linked Oligonucleotides Branched by a Pentaerythritol Linker and the Thermal Stabilities of the Triplexes with Single-Stranded DNA or RNA

Y Ueno, A Shibata, A Matsuda, Y Kitade - Bioconjugate chemistry, 2003 - ACS Publications
Synthesis of 3 '-3 '-linked oligonucleotides branched by a pentaerythritol linker is described.
The branched oligonucleotides were synthesized on a DNA/RNA synthesizer using a …

[引用][C] A convenient synthesis of 2−–5− linked oligoribonucleotides

Y Hayakawa, M Uchiyama, T Nobori, R Noyori - Tetrahedron letters, 1985 - Elsevier
NuOH: nucleosides Ar : phenyl, o-chlorophenyl, Page 1 Tetrahedron Letters,Vol.26,No.6,pp
761-764,1985 0040-4039185 $3.0~ + .oo Printed in Great Britain 01985 Pergamon Press Ltd …

Nucleosides and nucleotides. 162. Facile synthesis of 5′-5′-linked oligodeoxyribonucleotides with the potential for triple-helix formation

Y Ueno, A Ogawa, A Nakagawa, A Matsuda - Bioorganic & Medicinal …, 1996 - Elsevier
The facile synthesis of 5′-5′-linked oligodeoxyribonucleotides (ODNs) with the potential
for triple-helix formation is described. ODNs containing 5-trifluoroethoxycarbonyl-2 …