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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Grougnet, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Magiatis, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Mitaku, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Skaltsounis, A. L.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Cabalion, Pierre</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Tillequin, F.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Michel, S.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Dammarane triterpenes from Gardenia aubryi Vieill.</title>
        <secondary-title>Helvetica Chimica Acta</secondary-title>
      </titles>
      <pages>656-661</pages>
      <dates>
        <year>2011</year>
      </dates>
      <call-num>fdi:010053489</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Helvetica Chimica Acta</full-title>
      </periodical>
      <isbn>0018-019X</isbn>
      <accession-num>ISI:000289412900011</accession-num>
      <number>4</number>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010053489</url>
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          <url>https://www.documentation.ird.fr/intranet/publi/2011/05/010053489.pdf</url>
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      </urls>
      <volume>94</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Three new dammarane triterpenoids, gardaubryones A-C (1-3), were isolated from the gum collected on the aerial parts of Gardenia aubryi Vieill., together with the known compounds hydroxydammarenone II (4), ocotillone (5), cabraleone, and hollongdione. The structures of the novel compounds were established on the basis of mass spectrometry, NMR experiments, and chemical-correlation reactions.</abstract>
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