Pure and Applied Chemistry

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• Deb Indrajit, Sarzynska Joanna, Nilsson Lennart, Lahiri Ansuman: Conformational Preferences of Modified Uridines: Comparison of AMBER Derived Force Fields. J. Chem. Inf. Model. 2014, 140403141935006. <http://dx.doi.org/10.1021/ci400582a>
• Huang Ming, Giese Timothy J., Lee Tai-Sung, York Darrin M.: Improvement of DNA and RNA Sugar Pucker Profiles from Semiempirical Quantum Methods. J. Chem. Theory Comput. 2014, 10, 1538. <http://dx.doi.org/10.1021/ct401013s>
• Chiriac Aurica P., Nita Loredana E., Nistor Manuela T.: Nano-network with dual temperature and pH responsiveness based on copolymers of 2-hydroxyethyl methacrylate with 3,9-divinyl-2,4,8,10-tetraoxaspiro[5.5]-undecane. J  Nanopart Res 2011, 13, 6953. <http://dx.doi.org/10.1007/s11051-011-0605-7>
• Lahiri Ansuman, Sarzynska Joanna, Nilsson Lennart, Kulinski Tadeusz: Molecular dynamics simulation of the preferred conformations of 2-thiouridine in aqueous solution. Theor Chem Acc 2007, 117, 267. <http://dx.doi.org/10.1007/s00214-006-0141-1>
• Estévez Laura, González Moa María J., Terán Carmen, Mosquera Ricardo A.: Conformational study and electron density analysis of 9-[tetrahydropyran-3-yl]purine derivatives. Tetrahedron 2007, 63, 717. <http://dx.doi.org/10.1016/j.tet.2006.10.084>
• Paulini Ralph, Trindler Christian, Lerner Christian, Brändli Lukas, Schweizer W. Bernd, Jakob-Roetne Roland, Zürcher Gerhard, Borroni Edilio, Diederich François: Bisubstrate Inhibitors of CatecholO-Methyltransferase (COMT): the Crucial Role of the Ribose Structural Unit for Inhibitor Binding Affinity. ChemMedChem 2006, 1, 340. <http://dx.doi.org/10.1002/cmdc.200500065>
• Shishkin Oleg V., Gorb Leonid, Zhikol Oleg A., Leszczynski Jerzy: Conformational Analysis of Canonical 2-Deoxyribonucleotides. 1. Pyrimidine Nucleotides. J Biomol Struct Dyn 2004, 21, 537. <http://dx.doi.org/10.1080/07391102.2004.10506947>
• Lowary Todd L.: d-ARABINOFURANOSIDES FROM MYCOBACTERIA: SYNTHESIS AND CONFORMATION. J Carbohydr Chem 2002, 21, 691. <http://dx.doi.org/10.1081/CAR-120016487>
• Acharya Parag, Thibaudeau Christophe, Chattopadhyaya Jyoti: AN ENERGETIC CORRELATION OF AB INITIO AND NMR STUDIES OF THE 3′-GAUCHE EFFECT IN 3′-SUBSTITUTED THYMIDINES. NUCLEOT NUCL 2001, 20, 1229. <http://dx.doi.org/10.1081/NCN-100002524>
• Velikian Irina, Acharya Parag, Trifonova Anna, Földesi András, Chattopadhyaya Jyoti: The RNA molecular wire: the pH-dependent change of the electronic character of adenin-9-yl is transmitted to drive the sugar and phosphate torsions in adenosine 3′, 5′-bisphosphate. J Phys Org Chem 2000, 13, 300. <http://dx.doi.org/10.1002/1099-1395(200005)13:5<300::AID-POC245>3.0.CO;2-W>
• Acharya Parag, Trifonova Anna, Thibaudeau Christophe, Földesi András, Chattopadhyaya Jyoti: Die Übertragung des elektronischen Charakters von Guanin-9-yl bewirkt die Torsionen des Zucker-Phosphat-Rückgrats in Guanosin-3′,5′-bisphosphat. Angew Chem 1999, 111, 3861. <http://dx.doi.org/10.1002/(SICI)1521-3757(19991216)111:24<3861::AID-ANGE3861>3.0.CO;2-K>
• Marquez Victor E., Russ Pamela, Alonso Randolph, Siddiqui Maqbool A., Shin Kye-Jung, George Clifford, Nicklaus Marc C., Dai Fang, Ford Harry: Conformationally Restricted Nucleosides. The Reaction of Adenosine Deaminase with Substrates Built on a Bicyclo[3.1.0]hexane Template. Nucleosides and Nucleotides 1999, 18, 521. <http://dx.doi.org/10.1080/15257779908041487>
• Thibaudeau C., Nishizono N., Sumita Y., Matsuda A., Chattopadhyaya J.: Determination of the Group Electronegativity of CF₃ Group in 3′-O-CF₃-Thymidine by ¹-NMR. Nucleosides and Nucleotides 1999, 18, 1035. <http://dx.doi.org/10.1080/15257779908041642>
• Mernissi-Arifi Khalid, Schlewer Gilbert, Spiess Bernard: Inframolecular acid–base properties of myo-inositol 1,2,6-trisphosphate analogues: influence of the hydroxyl groups, phosphate configuration and intracyclic atom substitution. Carbohydrates Research 1998, 308, 9. <http://dx.doi.org/10.1016/S0008-6215(98)00060-3>
• Thibaudeau Christophe, Chattopadhyaya Jyoti: The Information Transmission from the Nucleobase Drives the Sugar-Phosphate Backbone Conformation in the Nucleotide Wire. Nucleosides and Nucleotides 1998, 17, 1589. <http://dx.doi.org/10.1080/07328319808004691>
• Luyten Ingrid, Matulic-Adamic Jasenka, Beigelman Leo, Chattopadhyaya Jyoti: The Electronic Nature of the Aglycone dictates the Drive of the Pseudorotational Equilibrium of the Pentofuranose Moiety in C-Nucleosides. Nucleosides and Nucleotides 1998, 17, 1605. <http://dx.doi.org/10.1080/07328319808004692>
• Berger I., Tereshko V., Ikeda H., Marquez V. E., Egli M.: Crystal structures of B-DNA with incorporated 2'-deoxy-2'-fluoro-arabino-furanosyl thymines: Implications of conformational preorganization for duplex stability. NucleicAcids Res 1998, 26, 2473. <http://dx.doi.org/10.1093/nar/26.10.2473>
• Luyten Ingrid, Thibaudeau Christophe, Sandström Anders, Chattopadhyaya Jyoti: The tunable transmission of the aromatic character of the aglycone through the anomeric effect in C-nucleosides drives its own sugar conformation: A thermodynamic study. Tetrahedron 1997, 53, 6433. <http://dx.doi.org/10.1016/S0040-4020(97)00302-5>
• Thibaudeau Christophe, Földesi András, Chattopadhyaya Jyoti: The first experimental evidence for a larger medium-dependent flexibility of natural β--nucleosides compared to the α--nucleosides. Tetrahedron 1997, 53, 14043. <http://dx.doi.org/10.1016/S0040-4020(97)00909-5>
• Thibaudeau C., Chattopadhyaya J.: The Discovery of Intramolecular Stereoelectronic Forces That Drive The Sugar Conformation in Nucleosides and Nucleotides. Nucleosides and Nucleotides 1997, 16, 523. <http://dx.doi.org/10.1080/07328319708002912>