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1 |
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 |
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Material Type: Artigo
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Practical and efficient synthesis of pyrano[3,2- c]pyridone, pyrano[4,3- b]pyran and their hybrids with nucleoside as potential antiviral and antileishmanial agentsFan, Xuesen ; Feng, Dong ; Qu, Yingying ; Zhang, Xinying ; Wang, Jianji ; Loiseau, Philippe M. ; Andrei, Graciela ; Snoeck, Robert ; Clercq, Erik DeBioorganic & medicinal chemistry letters, 2010-02, Vol.20 (3), p.809-813 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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The nucleoside analog clitocine is a potent and efficacious readthrough agentFriesen, Westley J ; Trotta, Christopher R ; Tomizawa, Yuki ; Zhuo, Jin ; Johnson, Briana ; Sierra, Jairo ; Roy, Bijoyita ; Weetall, Marla ; Hedrick, Jean ; Sheedy, Josephine ; Takasugi, James ; Moon, Young-Choon ; Babu, Suresh ; Baiazitov, Ramil ; Leszyk, John D ; Davis, Thomas W ; Colacino, Joseph M ; Peltz, Stuart W ; Welch, Ellen MRNA (Cambridge), 2017-04, Vol.23 (4), p.567-577 [Periódico revisado por pares]United States: Cold Spring Harbor Laboratory PressTexto completo disponível |
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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 |
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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 |
6 |
Material Type: Artigo
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Synthesis and anti-CVB3 activity of 4-amino acid derivative substituted pyrimidine nucleoside analoguesTao, Le ; Li, Yujiang ; Guo, Xiaohe ; Dong, Lihong ; Liu, Luping ; Wang, Qiang ; Yu, Xuejun ; Song, Chuanjun ; Chang, JunbiaoBioorganic & medicinal chemistry letters, 2020-01, Vol.30 (1), p.126770-126770, Article 126770 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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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 |
8 |
Material Type: Artigo
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Protection‐Free, Two‐step Synthesis of C5‐C Functionalized Pyrimidine NucleosidesPodskoczyj, Karolina ; Kuszczynska, Anna ; Dziergowska, Agnieszka ; Leszczynska, GrazynaCurrent protocols, 2024-02, Vol.4 (2), p.e984-n/aUnited StatesTexto completo disponível |
9 |
Material Type: Artigo
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Phosphonoamidate prodrugs of C5-substituted pyrimidine acyclic nucleosides for antiviral therapyPertusati, Fabrizio ; Serafini, Sara ; Albadry, Najmiyah ; Snoeck, Robert ; Andrei, GracielaAntiviral research, 2017-07, Vol.143, p.262-268 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
10 |
Material Type: Artigo
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Synthesis and evaluation of thymidine kinase 1-targeting carboranyl pyrimidine nucleoside analogs for boron neutron capture therapy of cancerAgarwal, Hitesh K. ; Khalil, Ahmed ; Ishita, Keisuke ; Yang, Weilian ; Nakkula, Robin J. ; Wu, Lai-Chu ; Ali, Tehane ; Tiwari, Rohit ; Byun, Youngjoo ; Barth, Rolf F. ; Tjarks, WernerEuropean journal of medicinal chemistry, 2015-07, Vol.100, p.197-209 [Periódico revisado por pares]France: Elsevier Masson SASTexto completo disponível |