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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%">Salas-Ambrosio, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Tronnet, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Since, M.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Bourgeade-Delmas, Sandra</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Stigliani, J. L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Vax, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Lecommandoux, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Dupuy, B.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Verhaeghe, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Bonduelle, C.</style>
          </author>
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      <titles>
        <title>Cyclic poly(alpha-peptoid)s by lithium bis(trimethylsilyl)amide (LiHMDS)-mediated ring-expansion polymerization : simple access to bioactive backbones</title>
        <secondary-title>Journal of the American Chemical Society</secondary-title>
      </titles>
      <pages>3697-3702</pages>
      <dates>
        <year>2021</year>
      </dates>
      <call-num>fdi:010081087</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Journal of the American Chemical Society</full-title>
      </periodical>
      <isbn>0002-7863</isbn>
      <accession-num>ISI:000630322300007</accession-num>
      <number>10</number>
      <electronic-resource-num>10.1021/jacs.0c13231</electronic-resource-num>
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          <url>https://www.documentation.ird.fr/hor/fdi:010081087</url>
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          <url>https://www.documentation.ird.fr/intranet/publi/2021/03/010081087.pdf</url>
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      <volume>143</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Cyclic polymers display unique physicochemical and biological properties. However, their development is often limited by their challenging preparation. In this work, we present a simple route to cyclic poly(alpha-peptoids) from N-alkylated-N-carboxyanhydrides (NNCA) using LiHMDS promoted ring-expansion polymerization (REP) in DMF. This new method allows the unprecedented use of lysine-like monomers in REP to design bioactive macrocycles bearing pharmaceutical potential against Clostridioides difficile, a bacterium responsible for nosocomial infections.</abstract>
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