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CCCC > Symposium Series > 2005, Volume 7, Collection Symposium Series

2005, Volume 7, Collection Symposium Series

ISBN	80-86241-25-4

Conference

Title	XIIIth Symposium on Chemistry of Nucleic Acid Components
Location	Špindlerův Mlýn
Date	3 Sep 2005 – 9 Sep 2005

Articles

• pp. 1-20
  Frank Seela, Xiaohua Peng, Hong Li, Padmaja Chittepu, Khalil I. Shaikh, Junlin He, Yang He and Igor Mikhailopulo Modified DNA: From synthesis to molecular recognition
• pp. 21-26
  Damian Ittig, Dorte Renneberg, David Vonlanthen, Samuel Luisier and Christian J. Leumann Oligonucleotide analogues: From supramolecular principles to biological properties
• pp. 27-28
  Patrick J. Hrdlicka, B. Ravindra Babu, Mads D. Sørensen, Niels Harrit and Jesper Wengel Ångström-scale chemical engineering: Multilabeled 2'-amino-LNA probes for nucleic acid detection in homogenous fluorescence assays
• pp. 29-37
  Piet Herdewijn The Diels–Alder cyclo addition as key reaction for the synthesis of cyclohexenyl nucleosides
• pp. 39-46
  Wojciech Dabkowski and Jan Michalski A novel approach to synthesis of nucleotides and their structural analogues via tricoordinate phosphorus reagents
• pp. 47-55
  Hans-Achim Wagenknecht Electron transfer chemistry in synthetically modified DNA
• pp. 57-64
  Isao Saito, Yoshio Saito, Akimitsu Okamoto, Tomohisa Ichiba, Keiichiro Kanatani and Kazuki Tainaka Design of highly selective fluorescent nucleobases for SNP typing: Base-discriminating fluorescent (BDF) probe
• pp. 65-73
  Eduard K. Liebler, Katrin B. Lorenz, Björn Dietrich, Katja Bensmann, Britta Eickmann and Ulf Diederichsen DNA binding of peptides derived from natural products or proteins and bending of DNA double strands
• pp. 75-76
  J. Chattopadhyaya Evidences for the electrostatic promoted modulation of the chemical reactivity of nucleobases and phosphates in RNA
• pp. 77-84
  Aaron M. Leconte and Floyd E. Romesberg Efforts towards expansion of the genetic alphabet
• pp. 85-85
  David C. K. Chu Dioxolane nucleosides: Chemistry and biology
• pp. 87-93
  Gloria Cristalli, Diego Dal Ben, Catia Lambertucci, Floriana R. Portino, Sara Taffi, Sauro Vittori and Rosaria Volpini Synthesis of new P2 receptor ligands
• pp. 95-103
  Karl Y. Hostetler and James R. Beadle Orally active lipid esters of antiviral nucleoside phosphonates
• pp. 105-113
  Chris Meier, Christian Ducho, Henning Jessen and Jan Balzarini Esterase-cleavable cycloSal-pronucleotides – the trapping concept
• pp. 115-122
  Shigeki Sasaki, Fumi Nagatsugi, Monsur Ali, Sayaka Mori and Shizuka Nakayama Molecular design for DNA hybridization-promoted reactions with high efficiency and selectivity
• pp. 123-126
  Andreas Marx Modulation of DNA polymerase function for DNA diagnostics
• pp. 127-132
  Sujiet Puthenveetil, Landon Whitby, Olena Maydanovych, Brittany Haudenschild and Peter A. Beal Modified RNA for the study of enzymes involved in RNA editing, the innate immune response and RNA interference
• pp. 133-142
  Agnieszka Bzowska, Katarzyna Stępniak, Monika Olasek, Maciej Długosz, Beata Wielgus-Kutrowska, Jan Antosiewicz, Antonín Holý, Gertraud Koellner, Albrecht Stroh, Grzegorz Raszewski, Thomas Steiner and Joachim Frank Attempts to differentiate subunits of trimeric and hexameric purine nucleoside phosphorylases by crystal structure and solution studies using purine bases, modified purine nucleosides, acyclonucleosides and their phosphonate analogues
• pp. 143-147
  Gaelle Deglane, Said Abes, Thibaut Michel, Alain Laurent, Magali Naval, Camille Martinand-Mari, Paul Prevot, Eric Vives, Ian Robbins, Ivan Barvik, Jr, Bernard Lebleu, Françoise Debart and Jean-Jacques Vasseur Combining a cationic phosphoramidate backbone and α-anomeric nucleosides provides oligonucleotides with improved hybridization and cell uptake properties
• pp. 149-152
  Fernando Ferreira, Albert Meyer, Jean-Jacques Vasseur and François Morvan Universal and reusable solide support thanks to a H-phosphonate diester linkage for the synthesis of single or multiple oligonucleotides
• pp. 153-157
  Ivan Rosenberg, Ivan Barvik, Miloš Buděšínský, Petr Kočalka, Šárka Králíková, Radek Liboska, Ondřej Pačes, Ondřej Páv, Magdalena Petrová, Radek Pohl, Martina Pressová, Dominik Rejman, Ivan Votruba and Zdeněk Točík Nucleoside phosphonic acids and related oligonucleotides: Structural diversity vs biological properties
• pp. 159-163
  Dominik Rejman, Petr Kočalka, Radek Pohl and Ivan Rosenberg Synthesis of 4'-N pyrrolidine nucleosides, nucleotides, and oligonucleotides
• pp. 165-166
  Radek Pohl, Dominik Rejman, Petr Kočalka and Ivan Rosenberg Pyrrolidine nucleotide analogues – conformation study
• pp. 167-171
  Piotr Guga, Anna Maciaszek and Wojciech J. Stec Oxathiaphospholane approach to the synthesis of oligodeoxyribonucleotides containing stereodefined internucleotide phosphoroselenoate function
• pp. 173-175
  Irene M. Lagoja "Split-nucleosides" – a novel class of purine bioisosters
• pp. 177-181
  Jerzy Boryski and Grzegorz Framski Mechanism of ribosylation of adenine
• pp. 183-187
  Michał Sobkowski, Jadwiga Jankowska, Jacek Stawinski and Adam Kraszewski Stereochemistry of internucleotide bond formation by the H-phosphonate method. 2. Transesterification of aryl ribonucleoside H-phosphonate diesters with alcohols
• pp. 189-193
  Johan Nilsson, Thomas Szabo, Gaston Lavén, Martin Kullberg, Adam Kraszewski and Jacek Stawinski Developing synthetic methods for bioactive phosphorus compounds. A progress report
• pp. 195-199
  Gaston Lavén and Jacek Stawinski Synthetic studies on the preparation of dinucleoside phenylphosphonates and phenylphosphonothioates via palladium(0) catalysed cross-coupling
• pp. 201-205
  Renata Hiresova, Liubov Putilova, Martin Kullberg and Jacek Stawinski Determination of absolute configuration of nucleoside 3'-H-phosphonothioate monoesters via stereochemical correlation analysis
• pp. 207-211
  Martin Kullberg and Jacek Stawinski Reactions of H-phosphonate and H-phosphonothioate diesters with carbonyl compounds. ³¹P NMR studies
• pp. 213-216
  Michal Hocek and Dana Hocková Regioselective cross-coupling reactions in the synthesis of multisubstituted purine bases and nucleosides
• pp. 217-220
  Petr Čapek and Michal Hocek Synthesis of (purin-6-yl)amino acids
• pp. 221-224
  Peter Šilhár, Radek Pohl, Ivan Votruba and Michal Hocek Synthesis and transformations of 6-(hydroxymethyl)purines
• pp. 225-228
  Pavol Cekan and Snorri Th. Sigurdsson Spin labeled nucleic acids for EPR spectroscopic study of DNA and RNA structure and function
• pp. 229-232
  Glenn A. Burley, Johannes Gierlich, Mohammad Reza Mofid, David M. Hammond and Thomas Carell New labelling strategies for the sensitive detection of nucleic acids
• pp. 233-237
  Gavin O'Mahony, Eleonor Ehrman and Morten Grøtli Adenosine-based fluorosides containing a novel heterocyclic ring system
• pp. 239-243
  Agnieszka B. Olejniczak, Błażej Wojtczak, Marzena Przepiórkiewicz, Marek Kwiatkowski and Zbigniew J. Lesnikowski Nucleosides and their phosphates modified with dicarba-closo-dodecaborane (–C₂B₁₀H₁₁) at 2'-position
• pp. 245-248
  Marie-Paule Teulade-Fichou, Markus Kaiser, Matthieu Sainlos, Sophie Bombard, David Monchaud, Clémence Jacquelin, Candide Hounsou and Rémy Lartia Customized fused aromatics for structural recognition of nucleic acids
• pp. 249-251
  Michal Česnek and Antonín Holý Biological activity of selected guanidinopurines
• pp. 253-257
  Matthaios Varaggoulis, Antonio Salgado and Thanasis Gimisis Synthesis and stability of parabanic acid nucleosides
• pp. 259-260
  Ulla Pentikäinen, Mikael Peräkylä and Harri Lönnberg The effect of base sequence on the hydrolytic stability of RNA phosphodiester bonds
• pp. 261-263
  Mikko Ora, Anu Kiviniemi, Tuomas Lönnberg, Sami Virtanen and Harri Lönnberg Phosphodiester cleavage of diribonucleoside 3',3'-monophosphates: Rate acceleration by the 2'-hydroxyl and 2'-amino function, implications to ribozyme action
• pp. 265-267
  Pasi Virta, Johanna Katajisto and Harri Lönnberg On-support oximation: A convenient method for solid-supported conjugation of oligonucleotides
• pp. 269-270
  Tuomas Lönnberg, Johanna Kiiski, Jonna Korhonen and Satu Mikkola The 2'-OH group as a hydrogen bond donor in the reactions of group I introns
• pp. 271-275
  Aleksandra Živković and Joachim W. Engels Fluorinated benzenes and benzimidazoles as RNA analogues
• pp. 277-278
  Jan Štambaský, Pavel Kočovský and Michal Hocek Towards a novel approach to C-nucleosides
• pp. 279-282
  Pavel Turek, Michal Hocek and Martin Kotora Cocyclotrimerization of 6-alkynylpurines with diynes as a novel approach to biologically active 6-arylpurines
• pp. 283-285
  Miroslav Otmar, Milena Masojídková and Antonín Holý Acyclic nucleoside phosphonates containing O-substituted hydroxypyridineamines and diamines as nucleobases
• pp. 287-290
  Marcela Krečmerová and Antonín Holý Synthesis of C-5 substituted HPMPC (cidofovir) derivatives
• pp. 291-295
  Karel Pomeisl, Ivan Votruba, Antonín Ho and Radek Pohl Pyrimidine 1-[2-(phosphonomethoxy)propyl] derivatives: Their syntheses and utilization as potent inhibitors of thymidine phosphorylase (PD-ECGF) from SD-lymphoma
• pp. 297-300
  Rosaria Volpini, Catia Lambertucci, Sara Taffi, Sauro Vittori, Karl-Norbert Klotz and Gloria Cristalli A₃ adenosine receptors: Synthesis and biological evaluation of new potent and selective ligands
• pp. 301-305
  Tomasz Goslinski, Grazyna Wenska and Bozenna Golankiewicz A novel series of strongly fluorescent tricyclic analogues of acyclovir resulting from spontaneous oxidation of some of their 7-[4-(benzhydryl)phenyl]-6-(4-R-phenyl) derivatives
• pp. 307-311
  Stephen L. Atkin, Sylvain Barrier, Stephen T. Beckett, Tom Brown, Grahame Mackenzie and Leigh Madden Towards the use of sporopollenin in drug delivery: Efficient encapsulation of oligonucleotides
• pp. 313-314
  Ineke Van Daele, Hélene Munier-Lehmann and Serge Van Calenbergh Exploring high affinity inhibitors of M. tuberculosis thymidiylate kinase
• pp. 315-318
  Kathleen Too, Daniel M. Brown and David Loakes Mutagenic nucleoside analogues for use as antivirals by error catastrophe
• pp. 319-327
  B.-K. Chun, J. L. Clark, J. Du, P. A. Furman, A. E. Hassan, L. Hollecker, T. McBrayer, M. E. Otto, K. W. Pankiewicz, S. E. Patterson, S. Rachakonda, R. F. Schinazi, L. J. Stuyver, P. W. Wang, K. A. Watanabe and T. Whitaker 5',9-Anhydro-3-(β-D-ribofuranosyl)purine nucleoside analogues as potential anti-HCV agents
• pp. 329-332
  Pooran Chand, Ajit K. Ghosh, Pravin L. Kotian, Tsu-Hsing Lin, Yahya El-Kattan, Minwan Wu, Vadlakonda S. Kumar and Yarlagadda S. Babu Synthesis of (2S,3S,4R,5R)-2-(4-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-5-(hydroxymethyl)-3-methylpyrrolidine-3,4-diol, an analog of potent HCV inhibitor
• pp. 333-337
  Sergey N. Mikhailov, Ekaterina V. Efimtseva, Alexandra A. Shelkunova, Jef Rozenski, Gert Emmerechts, Arthur Van Aerschot and Piet Herdewijn Chemical incorporation of minor tRNA component O-β-D-ribofuranosyl-(1''-2')-adenosine-5''-phosphate into oligoribonucleotides
• pp. 339-342
  Donata Pluskota-Karwatka, Magdalena Bruszyńska and Leif Kronberg Identification of an adduct formed in the reaction of malonaldehyde-glyoxal with adenosine
• pp. 343-346
  Thibaut Michel, Didier Gasparutto, Christine Saint-Pierre and Jean Cadet Synthesis of O⁶-hydroxyethyl-2'-deoxyguanosine adducts containing oligonucleotides for the evaluation of their mutagenic features
• pp. 347-350
  Sadie D. Osborne and Jane A. Grasby Investigations into substrate analogues for Fen-1
• pp. 351-354
  John A. Brazier, Julie Fisher and Richard Cosstick 3'-Phosphorothiolate linkages within multistranded helical structures
• pp. 355-359
  Marcin Kalek, Jacek Jemielity, Ewa Grudzien, Joanna Zuberek, Zbigniew M. Darzynkiewicz, Elzbieta Bojarska, Janusz Stępiński, Ryszard Stolarski, Richard E. Davis, Robert E. Rhoads and Edward Darżynkiewicz Synthesis and biochemical properties of the novel, enzymatically stable mRNA cap analogues with versatile potential applications
• pp. 361-365
  Jacek Jemielity, Janusz Stępiński, Joanna Zuberek, Ewa Grudzien, Magdalena Lewdorowicz, Ryszard Stolarski, Robert E. Rhoads and Edward Darżynkiewicz Dinucleotide analogues of the mRNA cap that enhance translational efficiency
• pp. 367-371
  Gabriela D. Ivanova, Andrey A. Arzumanov, B. Ravindra Babu, Neerja Karla, David Sweedler, Leo Beigelman, Jesper Wengel and Michael J. Gait Inhibition of HIV-1 Tat-dependent trans-activation by steric block oligonucleotide analogues containing amino modifications
• pp. 373-374
  Miroslav Hájek, Naděžda Matulová, Ivan Votruba, Antonín Holý and Eva Tloušťová Acyclic nucleoside phosphonates and human telomerase inhibition
• pp. 375-378
  Barbara Nawrot, Kinga Widera, Marzena Wojcik, Katarzyna Cieslinska, Beata Rebowska and Wojciech J. Stec Phosphorothioate modified DNAzymes
• pp. 379-380
  Andrey Semenyuk, András Földesi, Tommy Johansson, Camilla Estmer Nilsson, Mathias Brännvall, Leif Kirsebum and Marek Kwiatkowski Reliable method for RNA synthesis using t-butyldithiomethyl (DTM) group for the 2'-hydroxyl protection
• pp. 381-383
  Ludmila A. Alexandrova, Maxim V. Jasko and Marina K. Kukhanova Fluorescent esters of triphosphoric acid – effective substrates of terminal deoxynucleotidil transferase
• pp. 385-386
  Jelena Božilović, Jan W. Bats and Joachim W. Engels Synthesis and crystal structures of fluorinated indols as RNA analogues
• pp. 387-388
  Šárka Chalupová and Antonín Holý Synthesis of N⁴-substituted derivatives of (S)-1-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (HPMPC, Cidofovir, Vistide©)
• pp. 389-391
  Guido H. Clever and Thomas Carell Assembly of a highly DNA-duplex stabilizing salen-metallo-base pair
• pp. 393-394
  Liesbet Cosyn, Kenneth A. Jacobson and Serge Van Calenbergh 2-(1,2,3-Triazol-1-yl) N⁶-CH₃-substituted adenosine derivatives: Highly potent and selective A₃ receptor ligands
• pp. 395-396
  Petra Doláková, Milena Masojídková and Antonín Holý Synthesis and properties of chiral open-ring acyclic nucleoside bisphosphonates
• pp. 397-399
  Alexia Chollat-Namy, Didier Gasparutto, Jean Cadet and Alain Favier Nucleic acid biosensors for real-time monitoring of DNA repair activites by FRET
• pp. 401-402
  Imrich Géci, Vyacheslav V. Filichev and Erik B. Pedersen Synthesis of twisted intercalating nucleic acids (TINA) possesing acridine derivatives
• pp. 403-404
  Kateřina Hořejší, Radek Pohl and Antonín Holý Tricyclic etheno analogs of purines derived from 2-amino-6-chloropurine
• pp. 405-406
  Mariola Kozłowska and Zygmunt Kazimierczuk Synthesis of 2'-deoxyribonucleosides by the Mitsunobu reaction
• pp. 407-408
  Kaisa Ketomäki and Harri Lönnberg Selective oligonucleotide probes for detection of point mutations
• pp. 409-411
  Anastasia L. Khandazhinskaya, Elena A. Shirokova, Eugene A. Kataev, Sergey L. Deev, Eugene N. Ulomsky, Tatyana S. Shestakova, Vladimir L. Rusinov, Oleg N. Chupakhin, Eugene F. Belanov and Marina K. Kukhanova A new group of nucleoside mimics: Chemical synthesis and antiviral properties
• pp. 413-414
  Anu Kiviniemi, Petri Heinonen and Harri Lönnberg Synthesis of pentaerythritol-derived mass tags
• pp. 415-416
  Petr Kočalka, Markéta Rinnová, Václav Vaněk, Dominik Rejman, Ivan Votruba, Ivana Tomečková, Šárka Králíková, Magdalena Petrová, Ondřej Páv, Radek Pohl, Miloš Buděšínský, Radek Liboska, Zdeněk Točík and Ivan Rosenberg Novel nucleoside phosphonic acids-based inhibitors of thymidine phosphorylase
• pp. 417-419
  Joanna Kowalska, Magdalena Lewdorowicz, Joanna Zuberek, Elzbieta Bojarska, Zbigniew M. Darzynkiewicz, Ewa Grudzien, Richard E. Davis, Robert E. Rhoads, Janusz Stępiński, Ryszard Stolarski, Edward Darżynkiewicz and Jacek Jemielity Synthesis and properties of phosphorothioate 5' mRNA cap dinucleotides
• pp. 421-422
  Šárka Králíková, Miloš Buděšínský, Radek Liboska, Ondřej Páv and Ivan Rosenberg 2',5'-Linked oligo-3'-deoxynucleotide chimeras with chiral α-hydroxyphosphonate internucleotide linkage: Improvement of hybridisation selectivity toward RNA?
• pp. 423-424
  Martin Kuchař and Michal Hocek Synthesis of purines bearing functionalized C-substituents by nucleophilic additions to 6-ethynyl- or 6-vinylpurines
• pp. 425-427
  Irina V. Kulikova, Ivan S. Varizhuk, Georgii V. Bobkov, Ekaterina V. Efimtseva and Sergey N. Mikhailov Effective anomerisation of 2'-deoxyadenosine and thymidine derivatives
• pp. 429-431
  Peter Leonard, Xin Ming, Anup M. Jawalekar, Wilma Thür, Dieter Heindl and Frank Seela Universal bases: Base pairing and duplex stability of oligonucleotides containing pyrrolo[2,3-d]pyrimidines and 5-nitroindole nucleosides
• pp. 433-435
  Magdalena Lewdorowicz, Jacek Jemielity, Ryszard Kierzek, Michal Shapira, Janusz Stępiński, Ryszard Stolarski and Edward Darżynkiewicz Solid-supported synthesis of 5' mRNA cap-4 from trypanosomatides
• pp. 437-438
  Radek Liboska, Ondřej Páv and Ivan Rosenberg Monomers for novel phosphonate oligonucleotides, potential RNase L inhibitors
• pp. 439-440
  François Morvan, Aude-Emmanuelle Navarro, Cécile Dueymes, Ilaria Adamo, Andreas Schoenberger, Albert Meyer, Fritz Link, Meinolf Lange, Jean-Louis Imbach and Jean-Jacques Vasseur Solution phase synthesis of oligonucleotides by the phosphoramidite method using solid supported reagents
• pp. 441-442
  Radim Nencka, Ivan Votruba, Hubert Hřebabecký, Eva Tloušťová, Květa Horská, Milena Masojídková and Antonín Holý Design and synthesis of 5,6-disubstituted uracil derivatives as potent inhibitors of thymidine phosphorylase
• pp. 443-444
  Teija Niittymäki and Harri Lönnberg Sequence-selective cleavage of oligoribonucleotides
• pp. 445-446
  Petr Novák, Michal Hocek and Martin Kotora Synthesis of C-arylribosides by catalytic [2+2+2]-cyclotrimerization reaction
• pp. 447-448
  Ondřej Pačes and Ivan Rosenberg Isopolar, isosteric 4'-substituted 2',5'-oligoadenylates as potential RNase L activators
• pp. 449-451
  Dimitris Panagopoulos, Antonio Salgado and Thanasis Gimisis Preparation of 2'-deoxy nucleosides of cyanuric acid for their inclusion in DNA oligonucleotides
• pp. 453-454
  Ondřej Páv, Eva Protivínská, Jiří Jiráček and Ivan Rosenberg ABEI-labeled 2-5A: A way to chemiluminescent imaging of RNase L binding process
• pp. 455-456
  Agnieszka J. Pawłowicz, Tony Munter, Karel D. Klika and Leif Kronberg Reaction of acrolein with N⁹-ethyladenine – formation of adduct containing new six-membered fused rings
• pp. 457-459
  Päivi Poijärvi and Harri Lönnberg Biodegradable phosphate protections of oligonucleotides
• pp. 461-462
  Michal Šála, Hubert Hřebabecký, Milena Masojídková and Antonín Holý Synthesis of novel racemic conformationally locked carbocyclic nucleosides
• pp. 463-464
  Markéta Schinkmanová, Ivan Votruba and Antonín Holý N⁶-methyl-AMP hydrolase activates N⁶-substituted purine ANPs
• pp. 465-466
  Grigorii G. Sivets, Elena N. Kalinichenko and Igor A. Mikhailopulo Synthesis of 2'-β-fluoro-substituted adenine nucleosides via pivaloyl derivatives of adenosine and 3'-deoxyadenosine
• pp. 467-469
  Michał Sobkowski, Jacek Stawinski and Adam Kraszewski A proposal of D_P/L_P notation for nucleotide analogues with a chiral phosphorus centre
• pp. 471-473
  Damian Smuga, Iwona Fratczak and Elzbieta Sochacka Incorporation of amino acid modified nucleosides into catalytic core of deoxyribozyme "10-23"
• pp. 475-477
  Alicja Stachelska and Zbigniew Wieczorek Alkaline hydrolysis of the imidazole moiety in the dinucleotide cap analogs – is the stacking interaction important?
• pp. 479-480
  Janusz Stępiński, Remigiusz Worch, Joanna Zuberek, Elzbieta Bojarska, Jacek Jemielity, Magdalena Lewdorowicz, Ryszard Stolarski, Dorota Haber and Edward Darżynkiewicz Synthesis and preliminary characterization of mRNA 5' cap analogues containing ribavirin
• pp. 481-482
  Zdeněk Točík, Ivan Barvík, Jr., Miloš Buděšínský and Ivan Rosenberg Isosteric phosphonate 3'-O-P-CH₂-O-4'C internucleotide linkage: Attempts to get more data on its stereochemistry
• pp. 483-484
  Václav Vaněk, Miloš Buděšínský and Ivan Rosenberg The synthesis of monomers for prolinol-based oligonucleotides
• pp. 485-486
  Milan Vrabel, Ivan Rosenberg and Michal Hocek Synthesis of modified nucleosides and oligonucleotides bearing bipyridine or phenanthroline ligands
• pp. 487-488
  Silvie Vrbovská and Antonín Holý Novel type of bis-phosphonate congeners of acyclic nucleoside phosphonates
• pp. 489-491
  Borys Kierdaszuk and Jacek Wierzchowski 8-Azapurines as substrates for the E. coli purine nucleoside phosphorylase – II (xanthosine phosphorylase): Does the ribosylation always go to the aza-purine N(9)?
• pp. 493-494
  Gerda Wittel, Ping Gu and Joachim W. Engels Synthesis and activity of C-analogues for immune stimulating CpG-oligodeoxynucleotides

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