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      <title>Cyclic poly(alpha-peptoid)s by lithium bis(trimethylsilyl)amide (LiHMDS)-mediated ring-expansion polymerization : simple access to bioactive backbones</title>
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    <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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      <titleInfo>
        <title>Journal of the American Chemical Society</title>
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      <part>
        <detail type="volume">
          <number>143</number>
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        <detail type="volume">
          <number>10</number>
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        <extent unit="pages">
          <list> 3697-3702</list>
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        <dateIssued>2021</dateIssued>
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      <identifier type="issn">0002-7863</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010081087</identifier>
    <identifier type="doi">10.1021/jacs.0c13231</identifier>
    <identifier type="issn">0002-7863</identifier>
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      <recordCreationDate encoding="w3cdtf">2021-04-01</recordCreationDate>
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