Method for Synthesis of Enol Ester Functionalized Sulfonyl Fluorides

Herein, a novel, catalyst-free method for synthesizing enol ester functionalized sulfonyl fluorides is used using 2-chloroprop-2-ene-1-sulfonyl fluoride in a nucleophilic substitution with carboxylic acid derivatives. The method offers mild conditions, short reaction times, high purity, and efficient modification of drug candidates, advancing both organic synthesis and medicinal chemistry.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-06-29
DOI
https://doi.org/10.1021/acs.joc.5c00749
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Method for Synthesis of Enol Ester Functionalized Sulfonyl Fluorides

Hanadi A. Katouah, Eman Elsayed Fayad, Hua‐Li Qin, Monday Peter Ajisafe et al.
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
article

Method for Synthesis of Enol Ester Functionalized Sulfonyl Fluorides

Hanadi A. Katouah, Eman Elsayed Fayad, Hua‐Li Qin, Monday Peter Ajisafe, Heba H. Mohamedy
article en

Abstract

Herein, a novel, catalyst-free method for synthesizing enol ester functionalized sulfonyl fluorides is used using 2-chloroprop-2-ene-1-sulfonyl fluoride in a nucleophilic substitution with carboxylic acid derivatives. The method offers mild conditions, short reaction times, high purity, and efficient modification of drug candidates, advancing both organic synthesis and medicinal chemistry.

The Journal of Organic ChemistryVol. 90(27)
Taif University (SA), Wuhan University of Technology (CN), Umm al-Qura University (SA), Division of Chemistry (US), Division of Materials Science and Engineering (AU)
Taif University, Wuhan University of Technology
Openalex Percentile: Top 89%
Fluorine in Organic Chemistry
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Method for Synthesis of Enol Ester Functionalized Sulfonyl Fluorides — Hanadi A. Katouah, Eman Elsayed Fayad, et al. · The Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS