Disubstituted Meldrum’s Acid: Another Scaffold with SuFEx-like Reactivity

Sulfur Fluoride Exchange (SuFEx) chemistry represents an emerging class of click reactions that has found broad applications in drug discovery and materials science. Traditionally, SuFEx reactivity has been regarded as the exclusive privilege of sulfur and fluorine. Accordingly, the scaffolds exhibiting SuFEx-like reactivity without sulfur or fluorine have remained underdeveloped. Indeed, SuFEx reactions may represent a more generalizable mode of chemical reactivity. By enhancing the electrophilicity of the carbonyl group and increasing the steric hindrance around the carbon center, we identified disubstituted Meldrum's acid as a novel carbon-based scaffold with SuFEx-like reactivity. Various O-, S-, and N-nucleophiles are viable exchange partners in the presence of Barton's base or DBU. In addition to the original method, a catalytic protocol was developed and successfully applied to drug derivatization, including the gram-scale modification of acetaminophen.

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Publication Details

Journal
Molecules
Published
2025-08-29
DOI
https://doi.org/10.3390/molecules30173534
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Disubstituted Meldrum’s Acid: Another Scaffold with SuFEx-like Reactivity

Jiang Xie, Zhixiu Sun, Xiaoyan Peng, Le Li et al.
Molecules
Click Chemistry and Applications
article

Disubstituted Meldrum’s Acid: Another Scaffold with SuFEx-like Reactivity

Jiang Xie, Zhixiu Sun, Xiaoyan Peng, Le Li, Zhenguo Wang, Baoqi Chen
article en

Abstract

Sulfur Fluoride Exchange (SuFEx) chemistry represents an emerging class of click reactions that has found broad applications in drug discovery and materials science. Traditionally, SuFEx reactivity has been regarded as the exclusive privilege of sulfur and fluorine. Accordingly, the scaffolds exhibiting SuFEx-like reactivity without sulfur or fluorine have remained underdeveloped. Indeed, SuFEx reactions may represent a more generalizable mode of chemical reactivity. By enhancing the electrophilicity of the carbonyl group and increasing the steric hindrance around the carbon center, we identified disubstituted Meldrum's acid as a novel carbon-based scaffold with SuFEx-like reactivity. Various O-, S-, and N-nucleophiles are viable exchange partners in the presence of Barton's base or DBU. In addition to the original method, a catalytic protocol was developed and successfully applied to drug derivatization, including the gram-scale modification of acetaminophen.

MoleculesVol. 30(17)
Sun Yat-sen University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 83%
Click Chemistry and Applications
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Disubstituted Meldrum’s Acid: Another Scaffold with SuFEx-like Reactivity — Jiang Xie, Zhixiu Sun, et al. · Molecules (2025) | TGRS Research Map | TGRS