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        <identifier>oai:www.ideals.illinois.edu:2142/70240</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_14789</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:creator>Stevenson, Thomas Martin</dc:creator>
          <dc:date>2014-12-15T23:18:05Z</dc:date>
          <dc:date>2014-12-15T23:18:05Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1984</dc:date>
          <dc:date>1984</dc:date>
          <dc:description>Methods for the synthesis of 9-aminobenzimidazo{5,6-g}quinazoline (lin-naphthoadenine) and 9-amino-3-(beta)-D-ribofuranosylbenzimidazo{5,6-g}quinazoline (lin-naphthoadenosine) have been developed. The synthetic route commenced with 5,6-dimethylbenzimidazole and the linear array of rings was constructed by means of the Finkelstein reaction. lin-Naphthoadenosine was synthesized by ribosidation of 9-methylthiobenzimidazo{5,6-g}quinazoline followed by ammonia displacement. Syntheses of benzimidazo{5,6-g}-8H-quinazolin-9-one (lin-naphthohypoxanthine) and benzimidazo{5,6-g}-6H,8H-quinazoline-7,9-dione (lin-naphthoxanthine) were accomplished by similar routes. lin-Naphthoadenine and lin-naphthoadenosine were both found to be highly fluorescent. Neither of these purine analogs was found to be a substrate when tested for activity with the enzyme adenosine deaminase from calf intestinal mucosa.</dc:description>
          <dc:description>A synthetic route to imidazo{4,5-g}quinazolines (lin-benzopurines) reduced in the central ring has also been investigated. The first representative of this class of compounds, 4,7,8,9-tetrahydroimidazo{4,5-g}quinazoline-4,7-dione was synthesized from 1,3-diacetyl-4,5-dimethylimidazol-2-one in 5 steps utilizing the Finkelstein reaction to construct the tricyclic ring system.</dc:description>
          <dc:description>Made available in DSpace on 2014-12-15T23:18:05Z (GMT). No. of bitstreams: 1
8409838.pdf: 2878817 bytes, checksum: 74f1d82e709ec18aee7f477c310e32cd (MD5)
  Previous issue date: 1984</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 70406
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>122 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1984.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/70240</dc:identifier>
          <dc:identifier>(UMI)AAI8409838</dc:identifier>
          <dc:subject>Chemistry, Organic</dc:subject>
          <dc:title>Syntheses of Dimensionally Altered Enzyme Substrates by Means of the Finkelstein Reaction (Benzopurine, Naphthopurine)</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Chemistry</department>
            <discipline>Chemistry</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
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