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- Conversion of some pyrimidine 2′-deoxyribonucleosides into the corresponding 2′,3′-didehydro-2′,3′-dideoxynucleosides. Bhalchandra V. Joshi, T. Sudhakar Rao, Colin B. Reese
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 2537
- Synthesis of fluorescent 5-heteroarylpyrimidine-containing oligonucleotides via post-synthetic trifluoromethyl conversion. Yuta Ito, Hisato Tanaka, Ayana Murakami, Yasufumi Fuchi, Yoshiyuki Hari
, Org. Biomol. Chem.
, 2024
- Radiosynthesis of the anticancer nucleoside analogue Trifluridine using an automated 18F-trifluoromethylation procedure. Alice King, Andreas Doepner, David Turton, Daniela M. Ciobota, Chiara Da Pieve, Anne-Christine Wong Te Fong, Gabriela Kramer-Marek, Yuen-Li Chung, Graham Smith
, Org. Biomol. Chem.
, 2018
, 16
, 2986
- Review on fluorinated nucleoside/non-nucleoside FDA-approved antiviral drugs. Magda M. F. Ismail, Mohammed Salah Ayoup
, RSC Adv.
, 2022
, 12
, 31032
- Photo-cross-linking using trifluorothymidine and 3-cyanovinylcarbazole induced a large shifted 19F MR signal. Shigetaka Nakamura, Kenzo Fujimoto
, Chem. Commun.
, 2015
, 51
, 11765
- Guanidinatoaluminum complexes: synthesis, crystal structures and reactivities. Hong-Fei Han, Zhi-Qiang Guo, Shao-Feng Zhang, Jie Li, Xue-Hong Wei
, RSC Adv.
, 2016
, 6
, 101437
- Biocatalytic routes to anti-viral agents and their synthetic intermediates. Sjoerd Slagman, Wolf-Dieter Fessner
, Chem. Soc. Rev.
, 2021
, 50
, 1968
- Catalyst-free and visible light promoted trifluoromethylation and perfluoroalkylation of uracils and cytosines. Yang Huang, Yun-Yun Lei, Liang Zhao, Jiwei Gu, Qiuli Yao, Ze Wang, Xiao-Fei Li, Xingang Zhang, Chun-Yang He
, Chem. Commun.
, 2018
, 54
, 13662
- The isolation of high-affinity ssDNA aptamer for the detection of ribavirin in chicken. Mingyan Song, Chen Lyu, Nuo Duan, Shijia Wu, Imran Mahmood Khan, Zhouping Wang
, Anal. Methods
, 2021
, 13
, 3110
- Multiplexed detection of nucleic acids using 19F NMR chemical shift changes based on DNA photo-cross-linking of 3-vinylcarbazole derivatives. Shigetaka Nakamura, Yasuharu Takashima, Kenzo Fujimoto
, Org. Biomol. Chem.
, 2018
, 16
, 891