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- Total synthesis of pseudouridine via Heck-type C-glycosylation. Cheng-Ping Yu, Hsin-Yun Chang, Tun-Cheng Chien
, New J. Chem.
, 2019
, 43
, 8796
- Conversion of 2-deoxy-d-ribose into 2-amino-5-(2-deoxy-β-d-ribofuranosyl)pyridine, 2′-deoxypseudouridine, and other C-(2′-deoxyribonucleosides). Colin B. Reese, Qinpei Wu
, Org. Biomol. Chem.
, 2003
, 1
, 3160
- 2′-Deoxypseudouridine. Sydney D. Bridges, Daniel M. Brown, Richard C. Ogden
, J. Chem. Soc., Chem. Commun.
, 1977
, 460
- Pseudouridine transformations. Formation of 2′- and 3′-deoxypseudouridines via halogen intermediates using α-acetoxyisobutyryl chloride. Morris J. Robins, Wolfgang H. Muhs
, J. Chem. Soc., Chem. Commun.
, 1978
, 677
- DNA duplexes and triplex-forming oligodeoxynucleotides incorporating modified nucleosides forming stable and selective triplexes. Takashi Kanamori, Yoshiaki Masaki, Masahiro Mizuta, Hirosuke Tsunoda, Akihiro Ohkubo, Mitsuo Sekine, Kohji Seio
, Org. Biomol. Chem.
, 2012
, 10
, 1007
- Reaction mechanism of nucleoside 2′-deoxyribosyltransferases: free-energy landscape supports an oxocarbenium ion as the reaction intermediate. Jon del Arco, Almudena Perona, Leticia González, Jesús Fernández-Lucas, Federico Gago, Pedro A. Sánchez-Murcia
, Org. Biomol. Chem.
, 2019
, 17
, 7891
- The evolution of comprehensive strategies for furanoid glycal synthesis and their applications. Pinki Pal, Arun K. Shaw
, RSC Adv.
, 2017
, 7
, 25897
- Synthesis and triplex forming properties of pyrrolidino pseudoisocytidine containing oligodeoxynucleotides. Alain Mayer, Adrian Häberli, Christian J. Leumann
, Org. Biomol. Chem.
, 2005
, 3
, 1653