Original Papers- OKAMURA Hidenori -
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[2019]
1.Proto-Urea-RNA (Wöhler RNA) Containing Unusually Stable Urea Nucleosides.[Angewandte Chemie International Edition,58(51),(2019),18691-]Hidenori Okamura, Antony Crisp, Sarah Hübner, Sidney Becker, Petra Rov{\'{o}}, Thomas Carell
10.1002/anie.201911746
2.Proto‐Urea‐RNA (Wöhler RNA) Containing Unusually Stable Urea Nucleosides.[Angewandte Chemie,131(51),(2019),18864-]Hidenori Okamura, Antony Crisp, Sarah Hübner, Sidney Becker, Petra Rov{\'{o}}, Thomas Carell
10.1002/ange.201911746
3.Unified prebiotically plausible synthesis of pyrimidine and purine RNA ribonucleotides.[Science,366(6461),(2019),76-]Sidney Becker, Jonas Feldmann, Stefan Wiedemann, Hidenori Okamura, Christina Schneider, Katharina Iwan, Antony Crisp, Martin Rossa, Tynchtyk Amatov, Thomas Carell
10.1126/science.aax2747
4.A one-pot, water compatible synthesis of pyrimidine nucleobases under plausible prebiotic conditions.[Chemical Communications,(2019)]Hidenori Okamura, Sidney Becker, Niklas Tiede, Stefan Wiedemann, Jonas Feldmann, Thomas Carell
10.1039/c8cc09435g
[2018]
5.Modification of the aminopyridine unit of 2'-deoxyaminopyridinyl-pseudocytidine allowing triplex formation at CG interruptions in homopurine sequences..[Nucleic acids research,(2018)]Wang L, Taniguchi Y, Okamura H, Sasaki S
10.1093/nar/gky704
http://www.ncbi.nlm.nih.gov/pubmed/30102410
6.Stable and Selective Antiparallel Type Triplex DNA Formation by Targeting a GC Base Pair with the TFO Containing One N2-Phenyl-2′-deoxyguanosine.[Chemical & pharmaceutical bulletin,66(6),(2018),624-631]Taniguchi Y, Miyazaki M, Matsueda N, Wang L, Okamura H, Sasaki S
10.1248/cpb.c18-00043
http://www.ncbi.nlm.nih.gov/pubmed/29863064
7.Nicht-kanonische RNA-Nukleoside als molekulare Fossilien einer frühen Erde - Generierung durch präbiotische Methylierungen und Carbamoylierungen.[Angewandte Chemie,130(20),(2018),6050-]Christina Schneider, Sidney Becker, Hidenori Okamura, Antony Crisp, Tynchtyk Amatov, Michael Stadlmeier, Thomas Carell
10.1002/ange.201801919
8.Noncanonical RNA Nucleosides as Molecular Fossils of an Early Earth-Generation by Prebiotic Methylations and Carbamoylations.[Angewandte Chemie International Edition,57(20),(2018),5943-]Christina Schneider, Sidney Becker, Hidenori Okamura, Antony Crisp, Tynchtyk Amatov, Michael Stadlmeier, Thomas Carell
10.1002/anie.201801919
9.Wet-dry cycles enable the parallel origin of canonical and non-canonical nucleosides by continuous synthesis.[Nature Communications,9(1),(2018)]Sidney Becker, Christina Schneider, Hidenori Okamura, Antony Crisp, Tynchtyk Amatov, Milan Dejmek, Thomas Carell
10.1038/s41467-017-02639-1
10.A Click‐Chemistry Linked 2’3’‐cGAMP Analog.[Chemistry – A European Journal,(2018)]Clemens Reto Dialer, Samuele Stazzoni, David J. Drexler, Felix Moritz Müller, Simon Veth, Alexander Pichler, Hidenori Okamura, Gregor Witte, Karl-Peter Hopfner, Thomas Carell
10.1002/chem.201805409
http://www.ncbi.nlm.nih.gov/pubmed/30536650
[2017]
11.Effect of the 3-halo substitution of the 2 '-deoxy aminopyridinyl-pseudocytidine derivatives on the selectivity and stability of antiparallel triplex DNA with a CG inversion site.[BIOORGANIC & MEDICINAL CHEMISTRY,25(14),(2017),3853-3860]Lei Wang, Yosuke Taniguchi, Hidenori Okamura, Shigeki Sasaki
10.1016/j.bmc.2017.05.035
http://gateway.isiknowledge.com/gateway/Gateway.cgi?&GWVersion=2&SrcAuth=TohokuUniv&SrcApp=TohokuUniv&DestLinkType=FullRecord&KeyUT=WOS:000404087700028&DestApp=WOS
[2016]
12.Aminopyridinyl-Pseudodeoxycytidine Derivatives Selectively Stabilize Antiparallel Triplex DNA with Multiple CG Inversion Sites.[Angewandte Chemie,128(40),(2016),12633-]Hidenori Okamura, Yosuke Taniguchi, Shigeki Sasaki
10.1002/ange.201606136
13.Aminopyridinyl-Pseudodeoxycytidine Derivatives Selectively Stabilize Antiparallel Triplex DNA with Multiple CG Inversion Sites.[Angewandte Chemie International Edition,55(40),(2016),12445-]Hidenori Okamura, Yosuke Taniguchi, Shigeki Sasaki
10.1002/anie.201606136
[2015]
14.Enhancement of TFO Triplex Formation by Conjugation with Pyrene via Click Chemistry..[Chemical & Pharmaceutical Bulletin,63(11),(2015),920-926]Taniguchi Y, Tomizaki A, Matsueda N, Okamura H, Sasaki S, Chemical, pharmaceutical bulletin, vol. 63, no. 11, pp. 920-926
10.1248/cpb.c15-00570
http://www.ncbi.nlm.nih.gov/pubmed/26521856
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