Photoinduced PhI(OAc)<sub>2</sub>-Mediated Cross-Dehydrogenative Heteroarylation of Aldehydes

Direct acylation of heteroarenes with aldehydes has been established through a photoinduced hypervalent iodine-mediated cross-dehydrogenative coupling reaction. The reaction proceeds through the in situ generation of nucleophilic acyl radicals from aldehydes via acyl C-H hydrogen atom transfer (HAT), followed by a Minisci-type reaction with heteroarenes. The developed reaction system proved to be suitable for cross-coupling a diverse range of heterocycles and aldehydes.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-05-14
DOI
https://doi.org/10.1021/acs.joc.5c00655
Citations
4
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
3.74

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article

Photoinduced PhI(OAc)2-Mediated Cross-Dehydrogenative Heteroarylation of Aldehydes

Parthasarathy Gandeepan, Lusina Mantry
4 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
3.74
article

Photoinduced PhI(OAc)2-Mediated Cross-Dehydrogenative Heteroarylation of Aldehydes

Parthasarathy Gandeepan, Lusina Mantry
article en
4 citations

Abstract

Direct acylation of heteroarenes with aldehydes has been established through a photoinduced hypervalent iodine-mediated cross-dehydrogenative coupling reaction. The reaction proceeds through the in situ generation of nucleophilic acyl radicals from aldehydes via acyl C-H hydrogen atom transfer (HAT), followed by a Minisci-type reaction with heteroarenes. The developed reaction system proved to be suitable for cross-coupling a diverse range of heterocycles and aldehydes.

The Journal of Organic ChemistryVol. 90(20)
Indian Institute of Technology Tirupati (IN)
Ministry of Education, India, Science and Engineering Research Board
Openalex Percentile: Top 7%
Catalytic C–H Functionalization Methods
3.74
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