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        <datestamp>2026-09-29T16:09:53Z</datestamp>
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          <dc:title>Single-Atom
Nickel-Catalyzed C–H Amidation
of Pyridine and Quinoline N‑Oxides</dc:title>
          <dc:creator>Yijie Jiang (3797206)</dc:creator>
          <dc:creator>Yanze Lu (19337374)</dc:creator>
          <dc:creator>Haijing Li (197338)</dc:creator>
          <dc:creator>Conghui Tang (1608868)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Marine Biology</dc:subject>
          <dc:subject>Hematology</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>exafs analysis revealed</dc:subject>
          <dc:subject>efficient direct amidation</dc:subject>
          <dc:subject>commercially available quinoline</dc:subject>
          <dc:subject>heterogeneous nickel catalysis</dc:subject>
          <dc:subject>atom nickel catalyst</dc:subject>
          <dc:subject>4 &lt;/ sub</dc:subject>
          <dc:subject>pharmaceutically relevant 2</dc:subject>
          <dc:subject>atom nickel</dc:subject>
          <dc:subject>heterogeneous nature</dc:subject>
          <dc:subject>quinoline n</dc:subject>
          <dc:subject>work provides</dc:subject>
          <dc:subject>two one</dc:subject>
          <dc:subject>practical approach</dc:subject>
          <dc:subject>operational simplicity</dc:subject>
          <dc:subject>flexible preparation</dc:subject>
          <dc:subject>coordination environment</dc:subject>
          <dc:subject>catalytic system</dc:subject>
          <dc:subject>broad range</dc:subject>
          <dc:subject>aminoquinoline scaffolds</dc:subject>
          <dc:subject>also designed</dc:subject>
          <dc:description>A single-atom nickel catalyst (Ni-N-C-700) was developed
for the
efficient direct amidation of quinoline N-oxides with dioxazolones,
providing a broad range of 2-acetamidoquinoline N-oxide derivatives.
Two one-pot synthetic routes starting from commercially available
quinoline were also designed, enabling the flexible preparation of
both 2-acetamidoquinoline N-oxides and the pharmaceutically relevant
2-aminoquinoline scaffolds. The single-atom nickel catalyst showed
good stability, recyclability, and operational simplicity, while EXAFS
analysis revealed a well-defined Ni–N&lt;sub&gt;4&lt;/sub&gt; coordination
environment. A hot filtration experiment confirmed the heterogeneous
nature of the catalytic system. This work provides a practical approach
to the 2-acetamidoquinoline N-oxide and further illustrates the utility
of heterogeneous nickel catalysis in C–H functionalization
reactions.</dc:description>
          <dc:date>2026-09-29T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Journal contribution</dc:type>
          <dc:identifier>10.1021/acs.orglett.6c03895.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/journal_contribution/Single-Atom_Nickel-Catalyzed_C_H_Amidation_of_Pyridine_and_Quinoline_N_Oxides/34025034</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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