Asymmetric Photoredox Catalytic Minisci-Type Reactions of α-Bromide Amides

An asymmetric photoredox catalytic Minisci-type reaction between α-bromide amides and imine-containing azaarenes has been successfully developed. This catalyst system employs a chiral phosphoric acid alongside 3DPAFIPN as a photosensitizer. The reaction produces a diverse array of valuable amides, featuring azaarene-substituted tertiary carbon stereocenters at the β-position, in high yields (up to 85%) and good to excellent enantioselectivities (up to >99% enantiomeric excess (ee)). Importantly, this work marks the first example of asymmetric radical addition to simple azaarenes utilizing radicals functionalized with electron-withdrawing carbonyl groups, which are conventionally considered unfavorable for such transformations, especially in an enantioselective manner.

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Publication Details

Journal
Organic Letters
Published
2025-01-23
DOI
https://doi.org/10.1021/acs.orglett.4c04791
Citations
2
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Asymmetric Photoredox Catalytic Minisci-Type Reactions of α-Bromide Amides

Zhiyong Jiang, Yanli Yin, Qifu Li, Tianju Shao et al.
2 citations
Organic Letters
Radical Photochemical Reactions
1.87
article

Asymmetric Photoredox Catalytic Minisci-Type Reactions of α-Bromide Amides

Zhiyong Jiang, Yanli Yin, Qifu Li, Tianju Shao, Xiaowei Zhao
article en
2 citations

Abstract

An asymmetric photoredox catalytic Minisci-type reaction between α-bromide amides and imine-containing azaarenes has been successfully developed. This catalyst system employs a chiral phosphoric acid alongside 3DPAFIPN as a photosensitizer. The reaction produces a diverse array of valuable amides, featuring azaarene-substituted tertiary carbon stereocenters at the β-position, in high yields (up to 85%) and good to excellent enantioselectivities (up to >99% enantiomeric excess (ee)). Importantly, this work marks the first example of asymmetric radical addition to simple azaarenes utilizing radicals functionalized with electron-withdrawing carbonyl groups, which are conventionally considered unfavorable for such transformations, especially in an enantioselective manner.

Organic LettersVol. 27(5)
Henan University (CN), Henan Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 18%
Radical Photochemical Reactions
1.87
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