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1 |
Material Type: Artigo
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Unified prebiotically plausible synthesis of pyrimidine and purine RNA ribonucleotidesBecker, Sidney ; Feldmann, Jonas ; Wiedemann, Stefan ; Okamura, Hidenori ; Schneider, Christina ; Iwan, Katharina ; Crisp, Antony ; Rossa, Martin ; Amatov, Tynchtyk ; Carell, ThomasScience (American Association for the Advancement of Science), 2019-10, Vol.366 (6461), p.76-82 [Periódico revisado por pares]United States: The American Association for the Advancement of ScienceTexto completo disponível |
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Material Type: Artigo
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Selective prebiotic formation of RNA pyrimidine and DNA purine nucleosidesXu, Jianfeng ; Chmela, Václav ; Green, Nicholas J ; Russell, David A ; Janicki, Mikołaj J ; Góra, Robert W ; Szabla, Rafał ; Bond, Andrew D ; Sutherland, John DNature (London), 2020-06, Vol.582 (7810), p.60-66 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
3 |
Material Type: Artigo
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Catalytic C-H bond functionalisation of purine and pyrimidine nucleosides: a synthetic and mechanistic perspectiveGayakhe, Vijay ; Sanghvi, Yogesh S ; Fairlamb, Ian J. S ; Kapdi, Anant RChemical communications (Cambridge, England), 2015-08, Vol.51 (6), p.11944-1196 [Periódico revisado por pares]EnglandTexto completo disponível |
4 |
Material Type: Artigo
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Development of High‐Performance Pyrimidine Nucleoside and Oligonucleotide Diarylethene PhotoswitchesKolmar, Theresa ; Büllmann, Simon M. ; Sarter, Christopher ; Höfer, Katharina ; Jäschke, AndresAngewandte Chemie (International ed.), 2021-04, Vol.60 (15), p.8164-8173 [Periódico revisado por pares]Germany: Wiley Subscription Services, IncTexto completo disponível |
5 |
Material Type: Artigo
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Cu-mediated enamide formation in the total synthesis of complex peptide natural productsKuranaga, Takefumi ; Sesoko, Yusuke ; Inoue, MasayukiNatural product reports, 2014-01, Vol.31 (4), p.514-532 [Periódico revisado por pares]EnglandTexto completo disponível |
6 |
Material Type: Artigo
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Electron-Mediated Aminyl and Iminyl Radicals from C5 Azido-Modified Pyrimidine Nucleosides Augment Radiation Damage to Cancer CellsWen, Zhiwei ; Peng, Jufang ; Tuttle, Paloma R ; Ren, Yaou ; Garcia, Carol ; Debnath, Dipra ; Rishi, Sunny ; Hanson, Cameron ; Ward, Samuel ; Kumar, Anil ; Liu, Yanfeng ; Zhao, Weixi ; Glazer, Peter M ; Liu, Yuan ; Sevilla, Michael D ; Adhikary, Amitava ; Wnuk, Stanislaw FOrganic letters, 2018-12, Vol.20 (23), p.7400-7404 [Periódico revisado por pares]United States: American Chemical SocietyTexto completo disponível |
7 |
Material Type: Artigo
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Design and synthesis of novel 5-alkynyl pyrimidine nucleosides derivatives: Influence of C-6-substituent on antituberculosis activityVolov, Alexander N. ; Volov, Nikolai A. ; Platonova, Yana B.Bioorganic & medicinal chemistry letters, 2021-09, Vol.48, p.128261-128261, Article 128261 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
8 |
Material Type: Artigo
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Extension of furopyrimidine nucleosides with 5-alkynyl substituent: Synthesis, high fluorescence, and antiviral effect in the absence of free ribose hydroxyl groupsKaczmarek, Renata ; Twardy, Dylan J. ; Olson, Trevor L. ; Korczyński, Dariusz ; Andrei, Graciela ; Snoeck, Robert ; Dolot, Rafał ; Wheeler, Kraig A. ; Dembinski, RomanEuropean journal of medicinal chemistry, 2021-01, Vol.209, p.112884-112884, Article 112884 [Periódico revisado por pares]France: Elsevier Masson SASTexto completo disponível |
9 |
Material Type: Artigo
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Photoswitchable Formation of a DNA Interstrand Cross-Link by a Coumarin-Modified NucleotideHaque, Mohammad Mojibul ; Sun, Huabing ; Liu, Shuo ; Wang, Yinsheng ; Peng, XiaohuaAngewandte Chemie (International ed.), 2014-07, Vol.53 (27), p.7001-7005 [Periódico revisado por pares]Weinheim: WILEY-VCH VerlagTexto completo disponível |
10 |
Material Type: Artigo
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Chemo-enzymatic route to bridged homolyxofuranosyl-pyrimidinesKumar, Sandeep ; Singla, Harbansh ; Maity, Jyotirmoy ; Mangla, Priyanka ; Prasad, Ashok K.Carbohydrate research, 2020-06, Vol.492, p.108013-108013, Article 108013 [Periódico revisado por pares]Netherlands: Elsevier LtdTexto completo disponível |