<i>N</i> -Mesyl-Enabled Cu <sub>2</sub> O Catalysis: Synthesis of ( <i>E</i> )-3-Alkylideneisoindolin-1-ones and 3,4-Unsubstituted Isoquinolones via Sequential Alkynylation/Annulation

)-ones. Operationally simple and scalable, this method avoids expensive additives and offers a practical, selective entry to two privileged heterocyclic scaffolds.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-04-07
DOI
https://doi.org/10.1021/acs.joc.6c00362
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
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article

N -Mesyl-Enabled Cu 2 O Catalysis: Synthesis of ( E )-3-Alkylideneisoindolin-1-ones and 3,4-Unsubstituted Isoquinolones via Sequential Alkynylation/Annulation

Longqin Hu, Ahmed R. Ali
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

N -Mesyl-Enabled Cu 2 O Catalysis: Synthesis of ( E )-3-Alkylideneisoindolin-1-ones and 3,4-Unsubstituted Isoquinolones via Sequential Alkynylation/Annulation

Longqin Hu, Ahmed R. Ali
article en

Abstract

)-ones. Operationally simple and scalable, this method avoids expensive additives and offers a practical, selective entry to two privileged heterocyclic scaffolds.

The Journal of Organic ChemistryVol. 91(15)
Rutgers, The State University of New Jersey (US), Mansoura University (EG), Environmental and Occupational Health Sciences Institute (US), Medicina (PL), Rutgers Cancer Institute (US)
Openalex Percentile: Top 25%
Catalytic C–H Functionalization Methods
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