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  <title>Repository Collection: null</title>
  <link rel="alternate" href="https://scholar.dgist.ac.kr/handle/20.500.11750/56982" />
  <subtitle />
  <id>https://scholar.dgist.ac.kr/handle/20.500.11750/56982</id>
  <updated>2026-10-19T21:13:39Z</updated>
  <dc:date>2026-10-19T21:13:39Z</dc:date>
  <entry>
    <title>Equilibrium-driven decarbonylative multi-deuteration enables access to highly deuterated carbon frameworks</title>
    <link rel="alternate" href="https://scholar.dgist.ac.kr/handle/20.500.11750/60904" />
    <author>
      <name>Lee, Jiin</name>
    </author>
    <author>
      <name>Park, Taejun</name>
    </author>
    <author>
      <name>Park, Jeong Eun</name>
    </author>
    <author>
      <name>Moon, Hye Won</name>
    </author>
    <author>
      <name>Lee, Sunggi</name>
    </author>
    <id>https://scholar.dgist.ac.kr/handle/20.500.11750/60904</id>
    <updated>2026-09-29T06:10:14Z</updated>
    <published>2026-08-31T15:00:00Z</published>
    <summary type="text">Title: Equilibrium-driven decarbonylative multi-deuteration enables access to highly deuterated carbon frameworks
Author(s): Lee, Jiin; Park, Taejun; Park, Jeong Eun; Moon, Hye Won; Lee, Sunggi
Abstract: Deuterium incorporation is a powerful strategy for modulating metabolic stability and probing reaction mechanisms. However, existing approaches based on defunctionalization or hydrogen-deuterium exchange are typically limited to mono-deuteration or suffer from poor site selectivity, restricting access to multi-deuterated carbon centers. Herein, we report a cost-effective strategy for decarbonylative multi-deuteration of aldehydes by integrating polar alpha-deuteration, thiyl radical-mediated hydrogen atom transfer (HAT), and decarbonylative deuteration. A key feature of this approach is an equilibrium-controlled radical-polar process, in which multiple reversible steps are directed toward productive pathways through irreversible trapping of alkyl radicals. The method employs inexpensive, commercially available reagents and exhibits a broad substrate scope encompassing primary, secondary, and tertiary aldehydes, including structurally complex substrates. This strategy provides a practical platform for the synthesis of highly deuterated carbon frameworks, offering new opportunities for isotopic labeling and medicinal chemistry.</summary>
    <dc:date>2026-08-31T15:00:00Z</dc:date>
  </entry>
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