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        <datestamp>2024-06-20T06:50:17Z</datestamp>
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          <dc:title>Lactams. XX. Decarboxylation of Unsaturated Acids incorporated into Six-Membered Lactam Systems</dc:title>
          <dc:creator>Fujii, Tozo</dc:creator>
          <dc:creator>26775</dc:creator>
          <dc:creator>Ohba, Masashi</dc:creator>
          <dc:creator>26369</dc:creator>
          <dc:creator>60115219</dc:creator>
          <dc:creator>60115219</dc:creator>
          <dc:creator>Kogen, Hiroshi</dc:creator>
          <dc:creator>26776</dc:creator>
          <dc:creator>Ueda, Yuko</dc:creator>
          <dc:creator>26777</dc:creator>
          <dc:description>The thermal decarboxylation of some unsaturated acids (1,5,6,8,and 9) incorporated into six-membered lactams was examined. Although 8 and 9 did not undergo decarboxylation when heated neat at 175-180℃ and 240-245℃, respectively, for 2 h, 1,5,and 6 were decarboxylated in 1,1,2,2-tetrachloroethane at 135℃. The relative ease of the reaction was in the order of 1≥6≫5. In the case of 1,the rate-decreasing effects observed on dilution and on the addition of trichloroacetic acid suggest the reaction to be a dimeric intermolecular process.</dc:description>
          <dc:description>journal article</dc:description>
          <dc:publisher>日本薬学会</dc:publisher>
          <dc:date>1981-11-25</dc:date>
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          <dc:identifier>Chemical &amp; pharmaceutical bulletin</dc:identifier>
          <dc:identifier>11</dc:identifier>
          <dc:identifier>29</dc:identifier>
          <dc:identifier>3392</dc:identifier>
          <dc:identifier>3397</dc:identifier>
          <dc:identifier>AA00602100</dc:identifier>
          <dc:identifier>0009-2363</dc:identifier>
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          <dc:language>eng</dc:language>
          <dc:relation>10.1248/cpb.29.3392</dc:relation>
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