Oxidative Dearomative Coupling of Electron-Deficient Arenols Using Hypohalite Catalysis

We developed performant in situ hypohalite, especially hypobromite, catalysis for the oxidative dearomatization of low-reactivity electron-deficient arenols. The reaction scope encompasses inter- and intramolecular oxidative dearomative C-O, C-N, and C-C coupling reactions. Notably, using a chiral ammonium countercation, we achieved enantioselective hypobromite catalysis for oxidative dearomative coupling reactions. Mechanistic studies revealed that the reaction mechanisms might differ depending on the halide identity.

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Publication Details

Journal
Organic Letters
Published
2024-08-19
DOI
https://doi.org/10.1021/acs.orglett.4c02787
Citations
7
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
1.75

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article

Oxidative Dearomative Coupling of Electron-Deficient Arenols Using Hypohalite Catalysis

Takehiro Kato, Naoto Sahara, Kazuaki Ishihara, Muhammet Uyanik et al.
7 citations
Organic Letters
Oxidative Organic Chemistry Reactions
1.75
article

Oxidative Dearomative Coupling of Electron-Deficient Arenols Using Hypohalite Catalysis

Takehiro Kato, Naoto Sahara, Kazuaki Ishihara, Muhammet Uyanik, Sho Akagawa
article en
7 citations

Abstract

We developed performant in situ hypohalite, especially hypobromite, catalysis for the oxidative dearomatization of low-reactivity electron-deficient arenols. The reaction scope encompasses inter- and intramolecular oxidative dearomative C-O, C-N, and C-C coupling reactions. Notably, using a chiral ammonium countercation, we achieved enantioselective hypobromite catalysis for oxidative dearomative coupling reactions. Mechanistic studies revealed that the reaction mechanisms might differ depending on the halide identity.

Organic LettersVol. 26(34)
Nagoya University (JP)
Nagoya University, Japan Society for the Promotion of Science
Clean water and sanitation
Openalex Percentile: Top 17%
Oxidative Organic Chemistry Reactions
1.75
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