Green epoxidation of unactivated alkenes <i>via</i> the catalytic activation of hydrogen peroxide by 4-hydroxybenzaldehyde

An organocatalytic protocol that utilizes 4-hydroxybenzaldehyde as an activator of H 2 O 2 for the epoxidation of unactivated olefins is described. An unprecedented Payne/Dakin tandem mechanistic scenario is presented, supported by DI-HRMS experiments.

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Publication Details

Journal
Green Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5gc02537k
Citations
3
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
2.81

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article

Green epoxidation of unactivated alkenes via the catalytic activation of hydrogen peroxide by 4-hydroxybenzaldehyde

Christoforos G. Kokotos, Christiana Mantzourani, Efthymios T. Poursaitidis, Maroula G. Kokotou et al.
3 citations
Green Chemistry
Chemical Synthesis and Reactions
2.81
article

Green epoxidation of unactivated alkenes via the catalytic activation of hydrogen peroxide by 4-hydroxybenzaldehyde

Christoforos G. Kokotos, Christiana Mantzourani, Efthymios T. Poursaitidis, Maroula G. Kokotou, IERASIA TRIANTAFILLIDI
article en
3 citations

Abstract

An organocatalytic protocol that utilizes 4-hydroxybenzaldehyde as an activator of H 2 O 2 for the epoxidation of unactivated olefins is described. An unprecedented Payne/Dakin tandem mechanistic scenario is presented, supported by DI-HRMS experiments.

Green ChemistryVol. 27(36)
Agricultural University of Athens (GR), National and Kapodistrian University of Athens (GR)
Hellenic Foundation for Research and Innovation
Responsible consumption and production
Openalex Percentile: Top 10%
Chemical Synthesis and Reactions
2.81
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