A protocol for selective synthesis of thiol-functionalized allylic sulfonyl fluorides

An efficient and transition metal-free method has been established for synthesizing a class of novel thiol-functionalized allylic sulfonyl fluorides with exclusive regioselectivity. This method is distinguished by its broad functional group compatibility with up to 99% yield and mild reaction conditions. Additionally, subsequent SuFEx reactions and oxidation processes generated sulfonate, sulfoxide, and sulfone derivatives, which are key motifs in medicinal chemistry, with exceptional efficiency.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00487j
Citations
2
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
1.87

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article

A protocol for selective synthesis of thiol-functionalized allylic sulfonyl fluorides

Hanadi A. Katouah, Eman Elsayed Fayad, Hua‐Li Qin, Monday Peter Ajisafe et al.
2 citations
Organic & Biomolecular Chemistry
Sulfur-Based Synthesis Techniques
1.87
article

A protocol for selective synthesis of thiol-functionalized allylic sulfonyl fluorides

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

Abstract

An efficient and transition metal-free method has been established for synthesizing a class of novel thiol-functionalized allylic sulfonyl fluorides with exclusive regioselectivity. This method is distinguished by its broad functional group compatibility with up to 99% yield and mild reaction conditions. Additionally, subsequent SuFEx reactions and oxidation processes generated sulfonate, sulfoxide, and sulfone derivatives, which are key motifs in medicinal chemistry, with exceptional efficiency.

Organic & Biomolecular ChemistryVol. 23(23)
Taif University (SA), Wuhan University of Technology (CN), Umm al-Qura University (SA)
Taif University
Openalex Percentile: Top 16%
Sulfur-Based Synthesis Techniques
1.87
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