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        <identifier>oai:kanagawa-u.repo.nii.ac.jp:00002949</identifier>
        <datestamp>2023-05-15T16:35:02Z</datestamp>
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          <dc:title>Branched-chain Sugars. XXXV. The Synthesis of L-Rubranitrose (2,3,6-trideoxy-3-C-methyl-4-O-methyl-3-nitro-L-xylo-hexopyranose)</dc:title>
          <dc:creator>吉村, 寿次</dc:creator>
          <dc:creator>Yoshimura, Juji</dc:creator>
          <dc:creator>安盛, 俊雄</dc:creator>
          <dc:creator>Yasumori, Toshio</dc:creator>
          <dc:creator>Kondo, Tatsuya</dc:creator>
          <dc:creator>佐藤, 憲一</dc:creator>
          <dc:creator>Sato, Ken-ichi</dc:creator>
          <dc:description>The title compound was stereoselectively synthesized from methyl 2,6-dideoxy-4-O-methyl-β-L-thero-hexopyranosid-3-ulose (11) through the successive conversions; cyanomesylation, reductive spiro aziridine formation, reductive ring-opening to the methyl-branched amino sugar, oxidation to the corresponding nitro sugar.</dc:description>
          <dc:description>Article</dc:description>
          <dc:description>journal article</dc:description>
          <dc:publisher>日本化学会</dc:publisher>
          <dc:date>1984-09</dc:date>
          <dc:type>VoR</dc:type>
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          <dc:identifier>Bulletin of the Chemical Society of Japan</dc:identifier>
          <dc:identifier>9</dc:identifier>
          <dc:identifier>57</dc:identifier>
          <dc:identifier>2535</dc:identifier>
          <dc:identifier>2537</dc:identifier>
          <dc:identifier>AA00580132</dc:identifier>
          <dc:identifier>0009-2673</dc:identifier>
          <dc:identifier>https://kanagawa-u.repo.nii.ac.jp/record/2949/files/佐藤・化学-015.pdf</dc:identifier>
          <dc:identifier>http://hdl.handle.net/10487/8176</dc:identifier>
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          <dc:language>eng</dc:language>
          <dc:relation>10.1246/bcsj.57.2535</dc:relation>
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