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    <title>Repository Collection: null</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/56982</link>
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    <pubDate>Mon, 19 Oct 2026 21:12:59 GMT</pubDate>
    <dc:date>2026-10-19T21:12:59Z</dc:date>
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      <title>Equilibrium-driven decarbonylative multi-deuteration enables access to highly deuterated carbon frameworks</title>
      <link>https://scholar.dgist.ac.kr/handle/20.500.11750/60904</link>
      <description>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.</description>
      <pubDate>Mon, 31 Aug 2026 15:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://scholar.dgist.ac.kr/handle/20.500.11750/60904</guid>
      <dc:date>2026-08-31T15:00:00Z</dc:date>
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