Collection of Czechoslovak Chemical Communications - digital archive 

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• Tănase Constantin I., Drăghici Constantin, Cojocaru Ana, Galochkina Anastasia V., Orshanskaya Jana R., Zarubaev Vladimir V., Shova Sergiu, Enache Cristian, Maganu Maria: New carbocyclic N6-substituted adenine and pyrimidine nucleoside analogues with a bicyclo[2.2.1]heptane fragment as sugar moiety; synthesis, antiviral, anticancer activity and X-ray crystallography. Bioorganic & Medicinal Chemistry 2015, 23, 6346. <https://doi.org/10.1016/j.bmc.2015.08.033>
• Choi Won Jun, Ko Yun Jung, Chandra Girish, Lee Hyuk Woo, Kim Hea Ok, Koh Hyo Jung, Moon Hyung Ryong, Jung Young Hoon, Jeong Lak Shin: Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides. Tetrahedron 2012, 68, 1253. <https://doi.org/10.1016/j.tet.2011.11.052>
• Rejman Dominik, Pohl Radek, Dračínský Martin: The Synthesis and Conformation of Dihydroxypiperidinyl Derivates of Nucleobases as Novel Iminosugar Nucleoside Analogs. Eur J Org Chem 2011, 2011, 2172. <https://doi.org/10.1002/ejoc.201001610>
• Pohl Radek, Rulíšek Lubomír, Rejman Dominik: The stability and reactivity of activated acryloylcarbamates as reagents for the synthesis of N‐1 substituted thymine and uracil – an NMR and DFT study. J of Physical Organic Chem 2011, 24, 423. <https://doi.org/10.1002/poc.1775>
• Kovačková Soňa, Dračínský Martin, Rejman Dominik: The synthesis of piperidine nucleoside analogs—a comparison of several methods to access the introduction of nucleobases. Tetrahedron 2011, 67, 1485. <https://doi.org/10.1016/j.tet.2010.12.029>
• Hou Xiyan, Choi Won Jun, Phan Khai, Jacobson Kenneth A., Jeong Lak Shin, Choi Mun Ju, Chandra Girish, Lee Hyuk Woo: Regio- and stereoselective synthesis of truncated 3′-aminocarbanucleosides and their binding affinity at the A3 adenosine receptor. Biomol Chem 2011, 9, 6955. <https://doi.org/10.1039/c1ob05853c>
• Dejmek Milan, Hřebabecký Hubert, Dračínský Martin, Neyts Johan, Leyssen Pieter, Mertlíková-Kaiserová Helena, Nencka Radim: Conformationally locked nucleoside analogues based on the bridgehead substituted 7-oxonorbornane and their antiviral properties. Collect. Czech. Chem. Commun. 2011, 76, 1549. <https://doi.org/10.1135/cccc2011152>
• Šála Michal, De Palma Armando M., Hřebabecký Hubert, Nencka Radim, Dračínský Martin, Leyssen Pieter, Neyts Johan, Holý Antonín: Design, synthesis, and biological evaluation of novel coxsackievirus B3 inhibitors. Bioorganic & Medicinal Chemistry 2010, 18, 4374. <https://doi.org/10.1016/j.bmc.2010.04.081>
• Šála Michal, Hřebabecký Hubert, Dračínský Martin, Masojídková Milena, De Palma Armando M., Neyts Johan, Holý Antonín: Synthesis of novel racemic carbocyclic nucleosides derived from 5,6-disubstituted norbornene. Collect. Czech. Chem. Commun. 2010, 75, 1. <https://doi.org/10.1135/cccc2009116>
• Rejman Dominik, Kovačková Soňa, Pohl Radek, Dračínský Martin, Fiedler Pavel, Rosenberg Ivan: A convenient, high-yield synthesis of 1-substituted uracil and thymine derivatives. Tetrahedron 2009, 65, 8513. <https://doi.org/10.1016/j.tet.2009.08.019>
• Šála Michal, Hřebabecký Hubert, Dračínský Martin, Masojídková Milena, De Palma Armando M., Neyts Johan, Holý Antonín: Norbornane as the novel pseudoglycone moiety in nucleosides. Tetrahedron 2009, 65, 9291. <https://doi.org/10.1016/j.tet.2009.09.018>
• Hřebabecký Hubert, Dračínský Martin, De Palma Armando M., Neyts Johan, Holý Antonín: Synthesis of novel racemic carbocyclic nucleoside analogues derived from 4,8-dioxatricyclo[4.2.1.03,7]nonane-9-methanol and 4-oxatricyclo[4.3.1.03,7]decane-10-methanol, compounds with activity against Coxsackie viruses. Collect. Czech. Chem. Commun. 2009, 74, 469. <https://doi.org/10.1135/cccc2008193>
• Hřebabecký Hubert, Dračínský Martin, De Palma Armando M., Neyts Johan, Holý Antonín: Synthesis of novel carbocyclic nucleoside analogues derived from 7-oxabicyclo[2.2.1]heptane-2-methanol. Collect. Czech. Chem. Commun. 2009, 74, 487. <https://doi.org/10.1135/cccc2008204>
• Hřebabecký Hubert, Dračínský Martin, Holý Antonín: New carbocyclic nucleoside analogues built on a bicyclo[2.2.2]octane-2,2-dimethanol template. Collect. Czech. Chem. Commun. 2009, 74, 1425. <https://doi.org/10.1135/cccc2009090>
• Hřebabecký Hubert, Dračínský Martin, Holý Antonín: Synthesis of Novel Carbocyclic Nucleoside Analogues Containing Bicyclo[2.2.1]hept-2-ene-2-methanol. Collect. Czech. Chem. Commun. 2008, 73, 44. <https://doi.org/10.1135/cccc20080044>
• Hřebabecký Hubert, Dračínský Martin, Holý Antonín: Synthesis of Novel Carbocyclic Nucleosides and Pro-Tides Derived from 4-Oxatricyclo[4.2.1.03,7]nonane-9-methanol. Collect. Czech. Chem. Commun. 2007, 72, 1331. <https://doi.org/10.1135/cccc20071331>
• Dejmek Milan, Hřebabecký Hubert, Dračínský Martin, Holý Antonín: Synthesis of Novel Carbocyclic Nucleoside Analogues Derived from 2-(Hydroxymethyl)bicyclo[2.2.1]heptane. Collect. Czech. Chem. Commun. 2007, 72, 1523. <https://doi.org/10.1135/cccc20071523>
• Šála Michal, Hřebabecký Hubert, Masojídková Milena, Holý Antonín: Synthesis of Novel Racemic Conformationally Locked Carbocyclic Nucleosides Derived from 7-Substituted Bicyclo[2.2.1]hept-5-ene-2,2-dimethanols. Collect. Czech. Chem. Commun. 2006, 71, 635. <https://doi.org/10.1135/cccc20060635>
• Hřebabecký Hubert, Masojídková Milena, Dračínský Martin, Holý Antonín: Synthesis of Novel Conformationally Locked Carbocyclic Nucleosides Derived from 3-(Hydroxymethyl)bicyclo[2.2.1]heptane-2,5-diol. Collect. Czech. Chem. Commun. 2006, 71, 871. <https://doi.org/10.1135/cccc20060871>
• Hrebabecky Hubert, Masojidkova Milena, Holy Antonin: Synthesis of Novel Conformationally Locked Carbocyclic Nucleosides Derived from 5,5‐ and 6,6‐Bis(hydroxymethyl)bicyclo[2.2.1]heptan‐2‐ol. ChemInform 2005, 36. <https://doi.org/10.1002/chin.200540194>