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        <identifier>oai:www.ideals.illinois.edu:2142/20082</identifier>
        <datestamp>2023-07-10</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:contributor>Rinehart, Kenneth L., Jr.</dc:contributor>
          <dc:creator>Bible, Keith Christopher</dc:creator>
          <dc:date>2011-05-07T12:28:13Z</dc:date>
          <dc:date>2011-05-07T12:28:13Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1989</dc:date>
          <dc:description>Tunichlorin, a nickel chlorin isolated from the Caribbean tunicate Trididemnum solidum, has been identified as nickel (II) 2-devinyl-2-hydroxymethylpyropheophorbide a by chemical and spectroscopic methods. A partial synthesis of dimethyl tunichlorin from chlorophyll a (7 steps, 5% overall yield) has also confirmed the proposed structure. In the living tunicate, tunichlorin appears to exist primarily as a series of C-14 to C-18 ester homologues (principally tunichlorin-COO-(C$\sb3$H$\sb4$O)-(CH$\sb2$)$\sb{14}$CH$\sb3$). Preliminary studies suggest that tunichlorin esters are biosynthesized by the tunicate from alga-produced chlorophyll a. Although the biological function of tunichlorin esters remains unclear, analogy to related compounds suggests that they may be enzyme cofactors involved in reductive processes.</dc:description>
          <dc:description>In addition to tunichlorin and tunichlorin esters, examination of T. solidum extracts also revealed the presence of several known porphynoids, including chlorophyll a, pheophytin a, 10-hydroxypheophytin a, pheophorbide a, 10-hydroxypheophorbide a, pyropheophytin a, and 10-hydroxychlorophyll a. In addition, isopropyl pheophorbide a was identified from extracts of isopropyl alcohol-preserved tunicate, suggestive of an artifact of work-up and highlighting the pitfalls of natural product isolations. A previously unreported chlorophyll a degradation product, purpurin-18 phytyl ester, was also found in tunicate extracts.</dc:description>
          <dc:description>Made available in DSpace on 2011-05-07T12:28:13Z (GMT). No. of bitstreams: 2
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  Previous issue date: 1989</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:41:26Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:17:55-05:00
Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:identifier>AAI9010806</dc:identifier>
          <dc:identifier>(UMI)AAI9010806</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/20082</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:rights>Copyright 1989 Bible, Keith Christopher</dc:rights>
          <dc:subject>Chemistry, Biochemistry</dc:subject>
          <dc:subject>Chemistry, Organic</dc:subject>
          <dc:title>The porphynoid pigments of the Caribbean tunicate Trididemnum solidum</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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