Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1973, 38, 423-427
https://doi.org/10.1135/cccc19730423

Nucleic acid components and their analogues. CLV. Mechanism of anomalous opening of the O2,2'-anhydro bond in uracil cyclonucleosides

A. Holý

Crossref Cited-by Linking

  • Hu Shou‐Gang, Wu Yi‐Kang, Wu Yu‐Lin: A Concise Approach to the Synthesis of L‐ and Z)‐Deoxyribose. Chin. J. Chem. 2002, 20, 1358. <https://doi.org/10.1002/cjoc.20020201134>
  • Shi Zhen-Dan, Yang Bing-Hui, Wu Yu-Lin: A stereospecific synthesis of l-deoxyribose, l-ribose and l-ribosides. Tetrahedron 2002, 58, 3287. <https://doi.org/10.1016/S0040-4020(02)00230-2>
  • Santamaria F., Rayner B.: Improvements in the Synthesis of L-Ribonucleosides for the Preparation of Mirror-Image Oligoribonucleotides. Nucleosides and Nucleotides 1999, 18, 1405. <https://doi.org/10.1080/07328319908044733>
  • Jung Michael E., Nichols Christopher J.: A de novo synthesis of ethyl 2-deoxy-l-ribosides. Tetrahedron Letters 1998, 39, 4615. <https://doi.org/10.1016/S0040-4039(98)00852-1>
  • Pitsch Stefan: An Efficient Synthesis of Enantiomeric Ribonucleic Acids from D‐Glucose. Helvetica Chimica Acta 1997, 80, 2286. <https://doi.org/10.1002/hlca.19970800803>
  • Jung Michael E., Xu Yue: Efficient syntheses of l-ribose and 2-deoxy l-ribose from d-ribose and l-arabinose. Tetrahedron Letters 1997, 38, 4199. <https://doi.org/10.1016/S0040-4039(97)00870-8>
  • Ross Bruce S., Springer Robert H., Tortorici Zeb, Dimock Stuart: A Novel and Economical Synthesis of 2″-O-Alkyl-Uridines. Nucleosides and Nucleotides 1997, 16, 1641. <https://doi.org/10.1080/07328319708006245>
  • Faraj Abdesslem, Schinazi Raymond F., Xie Meng-Yu, Gosselin Gilles, Perigaud Christian, Imbach Jean-Louis, Sommadossi Jean-Pierre: Selective protection of toxicity of 2′,3′-dideoxypyrimidine nucleoside analogs by β-d-uridine in human granulocyte-macrophage progenitor cells. Antiviral Research 1996, 29, 261. <https://doi.org/10.1016/0166-3542(95)00905-1>
  • Nolte Alexis, Klußmann Sven, Bald Rolf, Erdmann Volker A., Fürste Jens P.: Mirror-design of L-oligonucleotide ligands binding to L-arginine. Nat Biotechnol 1996, 14, 1116. <https://doi.org/10.1038/nbt0996-1116>
  • König Joachim, Cech Dieter: Kurze Originalmitteilungen: über die Bildung von Cyclonucleosiden des 2‐Oxo‐4‐imidazolins. Zeitschrift fuer Chemie 1984, 24, 209. <https://doi.org/10.1002/zfch.19840240604>
  • Joecks A., Köppel H., Schleinitz K. D., Cech D.: NMR‐spektroskopische Untersuchungen zum Konformations‐verhalten von 2′‐ und 3′‐halogensubstituierten Pyrimidinnucleosiden. J. Prakt. Chem. 1983, 325, 881. <https://doi.org/10.1002/prac.19833250602>
  • Buchanan J.Grant, Clark David R.: Studies on the interconversion of 2,3'-anhydro-1-β-D-xylofuranosyluracil and 2,2'-anhydro-1-β-D-arabinofuranosyluracil. Carbohydrate Research 1979, 68, 331. <https://doi.org/10.1016/S0008-6215(00)83782-9>
  • HOLY A.: ChemInform Abstract: NUCLEINSAEURE‐KOMPONENTEN UND IHRE ANALOGEN 155. MITT. MECHANISMUS DER ANOMALEN OEFFNUNG DER O(2,2′)‐ANHYDROBINDUNG BEI URACIL‐CYCLONUCLEOSIDEN. Chemischer Informationsdienst 1973, 4. <https://doi.org/10.1002/chin.197318486>