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        <identifier>oai:figshare.com:article/34018245</identifier>
        <datestamp>2026-09-28T19:04:16Z</datestamp>
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          <dc:title>Transfer Hydrogenation
of Nitrones to Hydroxylamine
Derivatives with PhSiH&lt;sub&gt;3&lt;/sub&gt;</dc:title>
          <dc:creator>Wanzhen Guo (25133091)</dc:creator>
          <dc:creator>Xin Liu (43569)</dc:creator>
          <dc:creator>Xing Lu (1438414)</dc:creator>
          <dc:creator>Zhiqiang Ren (294429)</dc:creator>
          <dc:creator>Yuqi Zhang (286958)</dc:creator>
          <dc:creator>Bo Han (84102)</dc:creator>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>corresponding hydroxylamine derivatives</dc:subject>
          <dc:subject>3 &lt;/ sub</dc:subject>
          <dc:subject>readily available phsih</dc:subject>
          <dc:subject>hydroxylamine derivatives</dc:subject>
          <dc:subject>readily scalable</dc:subject>
          <dc:subject>wide range</dc:subject>
          <dc:subject>transfer hydrogenation</dc:subject>
          <dc:subject>sustainable strategy</dc:subject>
          <dc:subject>mild conditions</dc:subject>
          <dc:subject>hydrogen donor</dc:subject>
          <dc:subject>furan substituents</dc:subject>
          <dc:subject>free method</dc:subject>
          <dc:subject>findings demonstrated</dc:subject>
          <dc:subject>excellent yields</dc:subject>
          <dc:subject>effective conversion</dc:subject>
          <dc:subject>accommodating bromo</dc:subject>
          <dc:description>Herein, we report a practical metal- and additive-free
method for
transfer hydrogenation of nitrones, employing a readily available
PhSiH&lt;sub&gt;3&lt;/sub&gt; as the hydrogen donor. The findings demonstrated
the effective conversion of a wide range of ketone- and aldehyde-derived
nitrones into their corresponding hydroxylamine derivatives in good
to excellent yields under mild conditions. The reaction is readily
scalable and demonstrates broad functional group tolerance, accommodating
bromo, chloro, fluoro, trifluoromethyl, thioether, thiophene, and
furan substituents. Hence, the proposed operationally simple protocol
provides a practical and sustainable strategy, facilitating the synthesis
of structurally diverse hydroxylamine derivatives.</dc:description>
          <dc:date>2026-09-28T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Journal contribution</dc:type>
          <dc:identifier>10.1021/acs.orglett.6c03328.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/journal_contribution/Transfer_Hydrogenation_of_Nitrones_to_Hydroxylamine_Derivatives_with_PhSiH_sub_3_sub_/34018245</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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