“On-water” Photochemical Thiol-Ene Reaction of N-Enoxybenzotriazoles

Abstract We report herein a photochemical thiol-ene coupling using N-enoxybenzotriazoles, significantly accelerated under “on-water” conditions. This approach achieves efficient coupling within just five minutes via a remarkably rapid radical chain reaction, attributed to enhanced EDA formation and accelerated radical addition through a hydrophobic effect. The robustness of this method under various perturbation conditions underscores its potential for broad applications.

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Publication Details

Journal
Synthesis
Published
2025-06-06
DOI
https://doi.org/10.1055/a-2630-0528
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94

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article

“On-water” Photochemical Thiol-Ene Reaction of N-Enoxybenzotriazoles

Seunghoon Shin, Jun Sup Lee, Jin-Woo Jung
1 citations
Synthesis
Sulfur-Based Synthesis Techniques
0.94
article

“On-water” Photochemical Thiol-Ene Reaction of N-Enoxybenzotriazoles

Seunghoon Shin, Jun Sup Lee, Jin-Woo Jung
article en
1 citations

Abstract

Abstract We report herein a photochemical thiol-ene coupling using N-enoxybenzotriazoles, significantly accelerated under “on-water” conditions. This approach achieves efficient coupling within just five minutes via a remarkably rapid radical chain reaction, attributed to enhanced EDA formation and accelerated radical addition through a hydrophobic effect. The robustness of this method under various perturbation conditions underscores its potential for broad applications.

SynthesisVol. 57(20)
Yuhan University (KR), Hanyang University (KR)
National Research Foundation of Korea, Korea Drug Development Fund
Openalex Percentile: Top 25%
Sulfur-Based Synthesis Techniques
0.94
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