Base-Mediated Annulation Strategy to Naphthol Boronic Ester Derivatives

The base-promoted annulation reaction of homophthalic anhydrides with potassium ynone trifluoroborate salts offers a convenient method to access a range of <i>ortho</i>-acylphenol derivatives with complete regiocontrol. The products can be further functionalized chemoselectively by cross-coupling, O-alkylation, and oxidative coupling processes.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-24
DOI
https://doi.org/10.1021/acs.joc.5c02223
Citations
2
Primary Topic
Chemical synthesis and alkaloids
Type
article
Field-Weighted Citation Impact
1.87
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article

Base-Mediated Annulation Strategy to Naphthol Boronic Ester Derivatives

Joseph P. A. Harrity, Salah M. B. Obaida
2 citations
The Journal of Organic Chemistry
Chemical synthesis and alkaloids
1.87
article

Base-Mediated Annulation Strategy to Naphthol Boronic Ester Derivatives

Joseph P. A. Harrity, Salah M. B. Obaida
article en
2 citations

Abstract

The base-promoted annulation reaction of homophthalic anhydrides with potassium ynone trifluoroborate salts offers a convenient method to access a range of <i>ortho</i>-acylphenol derivatives with complete regiocontrol. The products can be further functionalized chemoselectively by cross-coupling, O-alkylation, and oxidative coupling processes.

The Journal of Organic ChemistryVol. 90(44)
Mustansiriyah University (IQ), Department of Mathematical Sciences (RU), Institute of Mathematical Statistics (US), University of Sheffield (GB)
Openalex Percentile: Top 13%
Chemical synthesis and alkaloids
1.87
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