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- The transition to magic bullets – transition state analogue drug design. Gary B. Evans, Vern L. Schramm, Peter C. Tyler
, Med. Chem. Commun.
, 2018
, 9
, 1983
- Synthesis and biological evaluation of unprecedented ring-expanded nucleosides (RENs) containing the imidazo[4,5-d][1,2,6]oxadiazepine ring system. Stefano D'Errico, Giorgia Oliviero, Jussara Amato, Nicola Borbone, Vincenzo Cerullo, Akseli Hemminki, Vincenzo Piccialli, Sabrina Zaccaria, Luciano Mayol, Gennaro Piccialli
, Chem. Commun.
, 2012
, 48
, 9310
- Purine nucleoside antibiotics: recent synthetic advances harnessing chemistry and biology. Jonas Motter, Caecilie M. M. Benckendorff, Sarah Westarp, Peter Sunde-Brown, Peter Neubauer, Anke Kurreck, Gavin J. Miller
, Nat. Prod. Rep.
, 2024
- Advances in 1,2,4-triazepines chemistry. Khaled M. Elattar, Mohamed A. Abozeid, Ibrahim A. Mousa, Ahmed El-Mekabaty
, RSC Adv.
, 2015
, 5
, 106710
- Copper-catalyzed three-component synthesis of 5-acetamidoimidazoles from carbodiimides, acyl chlorides and isocyanides. Giulia Sapuppo, Qian Wang, Dominique Swinnen, Jieping Zhu
, Org. Chem. Front.
, 2014
, 1
, 240
- The chemistry and biology of natural ribomimetics and related compounds. Takeshi Tsunoda, Samuel Tanoeyadi, Philip J. Proteau, Taifo Mahmud
, RSC Chem. Biol.
, 2022
, 3
, 519
- Synthesis of 3-(carboxyarylalkyl)imidazo[2,1-f][1,2,4]triazines as potential inhibitors of AMP deaminase. Joseph K. Kirkman, Stephen D. Lindell, Simon Maechling, Alexandra M. Z. Slawin, Christopher J. Moody
, Org. Biomol. Chem.
, 2008
, 6
, 4452
- First synthesis of bis[1,2,3]triazolo[1,5-b;5′,1′-f][1,3,6]thiadiazepine derivatives by [2+1] condensation of 1,2,3-thiadiazoles with vicinal diamines. Natalya N. Volkova, Evgeniy V. Tarasov, Vasiliy A. Bakulev, Wim Dehaen
, Chem. Commun.
, 1999
, 2273
- 8-Azapurines as isosteric purine fluorescent probes for nucleic acid and enzymatic research. Jacek Wierzchowski, Jan M. Antosiewicz, David Shugar
, Mol. BioSyst.
, 2014
, 10
, 2756
- Chapter 14. Nucleic acids. R. J. H. Davies
, Annu. Rep. Prog. Chem., Sect. B: Org. Chem.
, 1974
, 71
, 383