Synthesis of α,α‐Difluoroketones via Zinc‐Mediated Cross‐Electrophile Coupling of gem ‐Difluoroenol Sulfonates and N ‐(acyloxy)phthalimides

A zinc-mediated catalyst-free cross-electrophile coupling of gem-difluoroenol sulfonates with N-(acyloxy)phthalimides is developed. It efficiently affords diverse α,α-difluoroketones with broad radical compatibility, good gram-scale scalability, and functional group tolerance, enabling access to complex amino acid and glycosyl derivatives.

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Journal
ChemistryOpen
Published
2026-08-20
DOI
https://doi.org/10.1002/open.70285
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Synthesis of α,α‐Difluoroketones via Zinc‐Mediated Cross‐Electrophile Coupling of gem ‐Difluoroenol Sulfonates and N ‐(acyloxy)phthalimides

Huan Yang, Baojian Xiong, Xinmin Li, Jing Zhao et al.
ChemistryOpen
Fluorine in Organic Chemistry
article

Synthesis of α,α‐Difluoroketones via Zinc‐Mediated Cross‐Electrophile Coupling of gem ‐Difluoroenol Sulfonates and N ‐(acyloxy)phthalimides

Huan Yang, Baojian Xiong, Xinmin Li, Jing Zhao, Xiaohong Wang, Li Yang
article en

Abstract

A zinc-mediated catalyst-free cross-electrophile coupling of gem-difluoroenol sulfonates with N-(acyloxy)phthalimides is developed. It efficiently affords diverse α,α-difluoroketones with broad radical compatibility, good gram-scale scalability, and functional group tolerance, enabling access to complex amino acid and glycosyl derivatives.

ChemistryOpenVol. 15(9)
Zunyi Medical University (CN)
Openalex Percentile: Top 11%
Fluorine in Organic Chemistry
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