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 …
for triple-helix formation is described. ODNs containing 5-trifluoroethoxycarbonyl-2 …
Nucleosides and Nucleotides. 208. Alternate-Strand Triple-Helix Formation by the 3 '-3 '-Linked Oligodeoxynucleotides with the Anthraquinonyl Group at the Junction …
Y Ueno, M Mikawa, S Hoshika… - Bioconjugate Chemistry, 2001 - ACS Publications
The synthesis of 3 '-3 '-linked oligodeoxynucleotides (ODNs) with the anthraquinonyl group
at the junction point is described. The ODNs were synthesized on a DNA synthesizer using a …
at the junction point is described. The ODNs were synthesized on a DNA synthesizer using a …
Nucleosides and nucleotides. 127. A novel and convenient post-synthetic modification method for the synthesis of oligodeoxyribonucleotides carrying amino linkers at …
A Ono, N Haginoya, M Kiyokawa, N Minakawa… - Bioorganic & Medicinal …, 1994 - Elsevier
Methoxycarbonyl-2′-deoxyuridine has been synthesized and incorporated in
oligonucleotides. The fully protected oligonucleotides were treated with diaminoethane or …
oligonucleotides. The fully protected oligonucleotides were treated with diaminoethane or …
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 …
containing 2 '-deoxyuridines, modified at the 5-position by linkers ending with either one or …
[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 …
761-764,1985 0040-4039185 $3.0~ + .oo Printed in Great Britain 01985 Pergamon Press Ltd …
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 …
deoxyguanosine have been performed into a triple helix-forming oligodeoxyribonucleotide …
Synthesis of 2′-O, 3′-C-linked bicyclic nucleosides and bicyclic oligonucleotides
P Nielsen, HM Pfundheller, CE Olsen… - Journal of the Chemical …, 1997 - pubs.rsc.org
The 3′-C-allyl furanose 4 has been used as a precursor for synthesis of the novel 2′-O,
3′-C-linked bicyclic thymine nucleosides 15, 16, 20 and 25. The three bicyclic β …
3′-C-linked bicyclic thymine nucleosides 15, 16, 20 and 25. The three bicyclic β …
Triplex-forming ability of modified oligonucleotides
TH⊘ jland, BR Babu, T Bryld… - … , Nucleotides, and Nucleic …, 2007 - Taylor & Francis
We present our studies on the ability of several different nucleotide analogs as triplex-
forming oligonucleotides. The modifications tested include 4′-C-hydroxymethyl, LNA, 2 …
forming oligonucleotides. The modifications tested include 4′-C-hydroxymethyl, LNA, 2 …
Nucleosides and Nucleotides. 218. Alternate-Strand Triple-Helix Formation by the 3 '-3 '-Linked Oligodeoxynucleotides Using a Purine Motif
S Hoshika, Y Ueno, A Matsuda - Bioconjugate chemistry, 2003 - ACS Publications
In this paper, we describe the synthesis of the 3 '-3 '-linked TFOs that can form the
antiparallel triplexes with the duplex DNA target by reverse Hoogsteen hydrogen bonds …
antiparallel triplexes with the duplex DNA target by reverse Hoogsteen hydrogen bonds …
Post-synthetic functionalization of oligodeoxyribonucleotides at the 2′-position
H Ozaki, S Momiyama, K Yokotsuka, H Sawai - Tetrahedron Letters, 2001 - Elsevier
Post-synthetic functionalization of oligodeoxyribonucleotides at the 2′-position - ScienceDirect Skip
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