Ru-Catalyzed Redox-Neutral Coupling of <i>N</i>-Chlorobenzamides with Unsymmetrical Alkynes in Water

In water, Ru-catalyzed annulation of <i>N</i>-chlorobenzamides with unsymmetrical internal alkynes bearing aryl, hydroxy, ester, and sulfonyl functionalities has been accomplished to afford isoquinolone scaffolds under external oxidant-free conditions at room temperature. Use of water as reaction medium, redox-neutral conditions, regioselectivity, and substrate scope are important practical features.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-10-24
DOI
https://doi.org/10.1021/acs.joc.4c02234
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.75

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article

Ru-Catalyzed Redox-Neutral Coupling of N-Chlorobenzamides with Unsymmetrical Alkynes in Water

Tharmalingam Punniyamurthy, Sharajit Saha, Subhankar Dolai, Swati Samantaray et al.
3 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.75
article

Ru-Catalyzed Redox-Neutral Coupling of N-Chlorobenzamides with Unsymmetrical Alkynes in Water

Tharmalingam Punniyamurthy, Sharajit Saha, Subhankar Dolai, Swati Samantaray, Kshitiz Verma, Hemanga Bhattacharyya
article en
3 citations

Abstract

In water, Ru-catalyzed annulation of <i>N</i>-chlorobenzamides with unsymmetrical internal alkynes bearing aryl, hydroxy, ester, and sulfonyl functionalities has been accomplished to afford isoquinolone scaffolds under external oxidant-free conditions at room temperature. Use of water as reaction medium, redox-neutral conditions, regioselectivity, and substrate scope are important practical features.

The Journal of Organic ChemistryVol. 89(22)
Indian Institute of Technology Guwahati (IN)
Ministry of Education, India, Science and Engineering Research Board
Clean water and sanitation
Openalex Percentile: Top 32%
Catalytic C–H Functionalization Methods
0.75
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