Novel 2′-deoxycytidine analogues as pH independent substitutes of protonated cytosines in triple helix forming oligonucleotides

E Bédu, R Benhida, M Devys, JL Fourrey - Tetrahedron letters, 1999 - Elsevier
The N-acetyl derivatives 1a and 2a of the aminotriazole and aminoimidazole 2′-
deoxynucleosides 1 and 2 were synthesized as potential substitutes of protonated 2 …

Synthesis and properties of triple helix-forming oligodeoxyribonucleotides containing 7-chloro-7-deaza-2′-deoxyguanosine

Y Aubert, L Perrouault, C Hélène… - Bioorganic & medicinal …, 2001 - Elsevier
Multiple incorporations of 7-chloro-7-deaza-2′-deoxyguanosine in place of 2′-
deoxyguanosine have been performed into a triple helix-forming oligodeoxyribonucleotide …

Stabilization of DNA triplexes by dangling aromatic residues

M Kubota, A Ono - Tetrahedron letters, 2004 - Elsevier
Novel nucleoside analogues containing 2′-deoxyinosine and aromatic rings, which are
connected by short linker groups, were synthesized and incorporated into …

Properties of oligonucleotide with phenyl-substituted carbocyclic nucleoside analogs for the formation of duplex and triplex DNA

T Nasr, Y Taniguchi, T Takaki, H Okamura… - … and Nucleic Acids, 2012 - Taylor & Francis
(1 S, 3 S, 4 R)-1-Phenyl-1-thymidyl-3-hydroxy-4-hydroxymethylcyclopentane (10) and their
analogs were synthesized, incorporated into the oligodeoxynucleotides, and their properties …

Three new double-headed nucleotides with additional nucleobases connected to C-5 of pyrimidines; synthesis, duplex and triplex studies

P Kumar, PK Sharma, J Hansen, L Jedinak… - Bioorganic & Medicinal …, 2016 - Elsevier
In the search for double-coding DNA-systems, three new pyrimidine nucleosides, each
coded with an additional nucleobase anchored to the major groove face, are synthesized …

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 …

Oligo-2 '-deoxyribonucleotides Containing Uracil Modified at the 5-Position with Linkers Ending with Guanidinium Groups

V Roig, U Asseline - Journal of the American Chemical Society, 2003 - ACS Publications
We report here the synthesis and binding studies of oligo-2 '-deoxyribonucleotides (ODNs)
containing 2 '-deoxyuridines, modified at the 5-position by linkers ending with either one or …

Synthesis, Incorporation into Triplex-Forming Oligonucleotide, and Binding Properties of a Novel 2'-Deoxy-C-Nucleoside Featuring a 6-(Thiazolyl-5)benzimidazole …

D Guianvarc'h, JL Fourrey, R Maurisse, JS Sun… - Organic …, 2002 - ACS Publications
6-(Thiazolyl-5) benzimidazole (B t) was designed as a novel nucleobase for the specific
recognition of an inverted A⊙ T base pair in a triple helix motif. It was successfully …

Synthesis and duplex-forming ability of oligonucleotides containing 4′-carboxythymidine analogs

Y Hari, T Osawa, S Obika - Organic & biomolecular chemistry, 2012 - pubs.rsc.org
Oligonucleotides containing 4′-carboxy-, 4′-methoxycarbonyl-, 4′-carbamoyl-, and 4′-
methylcarbamoyl-thymidines, and their 2′-methoxy, 2′-amino or 2′-acetamido analogs …

A novel 2′-deoxynucleoside designed for enhanced recognition of AT Base-pairs

S Czernecki, A Hoang, JM Valéry - Tetrahedron letters, 1996 - Elsevier
A Novel 2’-Deoxynucleoside Designed for Enhanced Recognition of AT Base-pairs. Page 1
Tetrahedron Lerrers, Vol. 37, No. 49, pp. 8857-8860. 1996 Copyright 0 1996 Elsevier …