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    <pubDate>Fri, 31 Aug 2012 15:19:40 +0200</pubDate>
    <lastBuildDate>Fri, 31 Aug 2012 15:19:40 +0200</lastBuildDate>
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      <title>Synthesis of 1,4-Disubstituted Mono and Bis-triazolocarbo-acyclonucleoside Analogues of 9-(4-Hydroxybutyl)guanine by Cu(I)-Catalyzed Click Azide-Alkyne Cycloaddition</title>
      <link>http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/25939</link>
      <description>A series of novel mono-1,2,3-triazole and bis-1,2,3-triazole acyclonucleoside analogues of 9-(4-hydroxybutyl)guanine was prepared via copper(I)-catalyzed 1,3-dipolar cycloaddition of N-9 propargylpurine, N-1-propargylpyrimidines/as-triazine with the azido-pseudo-sugar 4-azidobutylacetate under solvent-free microwave conditions, followed by treatment with K2CO3/MeOH, or NH3/MeOH. All compounds studied in this work were screened for their antiviral activities [against human rhinovirus (HRV) and hepatitis C virus (HCV)] and antibacterial activities against a series of Gram positive and negative bacteria.</description>
      <author>Jamal Krim; Mohamed Taourirte; Joachim W. Engels</author>
      <category>article</category>
      <guid>http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/25939</guid>
      <pubDate>Fri, 31 Aug 2012 15:19:40 +0200</pubDate>
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