Visible-Light-Induced Acridinium-Catalyzed Acylation of Isoquinolines with Aldehydes via HAT

Abstract A novel synthetic method utilizes visible light to promote acridinium-catalyzed acylation of substituted isoquinoline via aldehydes in an air atmosphere at room temperature is reported. This method involves the formation of C–C bonds to synthesize the desired product with an excellent yield. This organophotoredox-catalyzed, transition-metal-free synthetic process provides the target compounds in an immensely sustainable manner despite tolerating a broad range of functional groups.

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Publication Details

Journal
Synlett
Published
2024-12-11
DOI
https://doi.org/10.1055/a-2500-6651
Citations
5
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.25
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article

Visible-Light-Induced Acridinium-Catalyzed Acylation of Isoquinolines with Aldehydes via HAT

Satya P. Singh, Mangla Mishra, Vishal Srivastava, Shraddha Tivari et al.
5 citations
Synlett
Radical Photochemical Reactions
1.25
article

Visible-Light-Induced Acridinium-Catalyzed Acylation of Isoquinolines with Aldehydes via HAT

Satya P. Singh, Mangla Mishra, Vishal Srivastava, Shraddha Tivari, Praveen P. Singh, Pravin K. Singh
article en
5 citations

Abstract

Abstract A novel synthetic method utilizes visible light to promote acridinium-catalyzed acylation of substituted isoquinoline via aldehydes in an air atmosphere at room temperature is reported. This method involves the formation of C–C bonds to synthesize the desired product with an excellent yield. This organophotoredox-catalyzed, transition-metal-free synthetic process provides the target compounds in an immensely sustainable manner despite tolerating a broad range of functional groups.

SynlettVol. 36(08)
University of Allahabad (IN), Department of Physics, Mathematics and Informatics (BY)
Responsible consumption and production
Openalex Percentile: Top 22%
Radical Photochemical Reactions
1.25
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