Photoredox‐Catalyzed α‐Arylation of Bromotrifluoroacetone with Electron‐Rich (Hetero)Arenes

Abstract Photoredox‐catalyzed radical addition of bromotrifluoroacetone and (hetero)arenes to carbonyl compounds has been established under mild conditions. The proposed method enables the synthesis of valuable α‐aryl trifluoromethyl ketone compounds, including biologically relevant arene derivatives, with good yields and regioselectivities. This method eliminates competitive bromination using Zn(OAc) 2 as an additive.

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Publication Details

Journal
ChemistrySelect
Published
2025-05-28
DOI
https://doi.org/10.1002/slct.202502626
Citations
2
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Photoredox‐Catalyzed α‐Arylation of Bromotrifluoroacetone with Electron‐Rich (Hetero)Arenes

Satoshi Mizuta, Tomoko Yamaguchi, Takeshi Ishikawa, Masaharu Iwasaki
2 citations
ChemistrySelect
Radical Photochemical Reactions
1.87
article

Photoredox‐Catalyzed α‐Arylation of Bromotrifluoroacetone with Electron‐Rich (Hetero)Arenes

Satoshi Mizuta, Tomoko Yamaguchi, Takeshi Ishikawa, Masaharu Iwasaki
article en
2 citations

Abstract

Abstract Photoredox‐catalyzed radical addition of bromotrifluoroacetone and (hetero)arenes to carbonyl compounds has been established under mild conditions. The proposed method enables the synthesis of valuable α‐aryl trifluoromethyl ketone compounds, including biologically relevant arene derivatives, with good yields and regioselectivities. This method eliminates competitive bromination using Zn(OAc) 2 as an additive.

ChemistrySelectVol. 10(21)
Kagoshima University (JP), Nagasaki University (JP), The University of Osaka (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science
Openalex Percentile: Top 15%
Radical Photochemical Reactions
1.87
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