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        <datestamp>2026-09-25T09:05:21Z</datestamp>
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          <dc:title>A General Route
to Silacyclohexanones via Regioselective
Copper-Catalyzed Borylative Cyclization</dc:title>
          <dc:creator>Chen-Li Jin (20401509)</dc:creator>
          <dc:creator>Ting Wu (106368)</dc:creator>
          <dc:creator>Rong-Jun Shi (25108574)</dc:creator>
          <dc:creator>Hui-Ting Chen (327178)</dc:creator>
          <dc:creator>Jun-Han Ma (16438743)</dc:creator>
          <dc:creator>Zheng Xu (162992)</dc:creator>
          <dc:creator>Li-Wen Xu (572954)</dc:creator>
          <dc:creator>Fei Ye (339913)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Evolutionary Biology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>step oxidation sequence</dc:subject>
          <dc:subject>reaction proceeds via</dc:subject>
          <dc:subject>dft calculations corroborate</dc:subject>
          <dc:subject>catalyzed borylative cyclization</dc:subject>
          <dc:subject>broad substrate scope</dc:subject>
          <dc:subject>&gt;- selective cyclization</dc:subject>
          <dc:subject>wittig olefination</dc:subject>
          <dc:subject>synthetic utility</dc:subject>
          <dc:subject>silicon center</dc:subject>
          <dc:subject>silacyclohexyl boronates</dc:subject>
          <dc:subject>scale capability</dc:subject>
          <dc:subject>observed selectivity</dc:subject>
          <dc:subject>membered rings</dc:subject>
          <dc:subject>including ketalization</dc:subject>
          <dc:subject>general route</dc:subject>
          <dc:subject>endo &lt;/</dc:subject>
          <dc:subject>diverse transformations</dc:subject>
          <dc:subject>deliver 4</dc:subject>
          <dc:subject>conformational role</dc:subject>
          <dc:subject>chloromethyl butenylsilanes</dc:subject>
          <dc:subject>afford 4</dc:subject>
          <dc:description>A copper-catalyzed regioselective
borylative cyclization of chloromethyl
butenylsilanes with bis(pinacolato)diboron has been reported. The
reaction proceeds via an &lt;i&gt;endo&lt;/i&gt;-selective cyclization
to deliver 4-silacyclohexyl boronates, which undergo a two-step oxidation
sequence to afford 4-silacyclohexanones. DFT calculations corroborate
the observed selectivity, highlighting the conformational role of
the silicon center in favoring the six-membered rings. This protocol
features readily available starting materials, a broad substrate scope,
good functional group tolerance, and gram-scale capability. The synthetic
utility of the resulting silacyclohexanones is demonstrated through
diverse transformations, including ketalization, allylation, Wittig
olefination, and Baeyer–Villiger oxidation.</dc:description>
          <dc:date>2026-09-25T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1021/acs.orglett.6c03675.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/A_General_Route_to_Silacyclohexanones_via_Regioselective_Copper-Catalyzed_Borylative_Cyclization/33994206</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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