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          <dc:title>Germyl Radical Cyclization
of N‑Propargyl
Aromatic Amines with Germanes: A Concise Route to Germanium-Containing
Quinolines</dc:title>
          <dc:creator>Yue Zhang (30585)</dc:creator>
          <dc:creator>Yanjun Wu (418662)</dc:creator>
          <dc:creator>Haibin Xiao (1583728)</dc:creator>
          <dc:creator>Junhao Chen (4689715)</dc:creator>
          <dc:creator>Zihan Wu (8492130)</dc:creator>
          <dc:creator>Xiaolei Huang (1397371)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Neuroscience</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Sociology</dc:subject>
          <dc:subject>Information Systems not elsewhere classified</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Mental Health</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>transformation proceeds via</dc:subject>
          <dc:subject>mechanistic investigations indicate</dc:subject>
          <dc:subject>features high regioselectivity</dc:subject>
          <dc:subject>enabling efficient construction</dc:subject>
          <dc:subject>broad substrate scope</dc:subject>
          <dc:subject>germyl radical cyclization</dc:subject>
          <dc:subject>radical pathway</dc:subject>
          <dc:subject>substituted quinolines</dc:subject>
          <dc:subject>remained unexplored</dc:subject>
          <dc:subject>privileged class</dc:subject>
          <dc:subject>n &lt;/</dc:subject>
          <dc:subject>marketed pharmaceuticals</dc:subject>
          <dc:subject>dilauroyl peroxide</dc:subject>
          <dc:subject>determining step</dc:subject>
          <dc:subject>concise route</dc:subject>
          <dc:description>Quinolines represent a privileged class of heterocyclic
scaffolds
widely prevalent in biologically active natural products and marketed
pharmaceuticals. Despite their significance, the synthesis of germanium-substituted
quinolines through germyl radical cyclization has remained unexplored
to date. Herein, we report a dilauroyl peroxide (LPO)-mediated cascade
protocol involving germylation, cyclization, and aromatization of &lt;i&gt;N&lt;/i&gt;-propargyl aromatic amines with germanes, enabling efficient
construction of 3-germanium-substituted quinolines. This transformation
proceeds via a radical pathway and features high regioselectivity,
broad substrate scope, and good functional group compatibility. Mechanistic
investigations indicate that cleavage of the Ge–H bond serves
as the rate-determining step.</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.joc.6c01998.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/journal_contribution/Germyl_Radical_Cyclization_of_N_Propargyl_Aromatic_Amines_with_Germanes_A_Concise_Route_to_Germanium-Containing_Quinolines/34027687</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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