Expedient access to α-(hetero)aryl-α-keto-1,3-diamines <i>via</i> redox-neutral photocatalyzed reactions of <i>N</i>-vinylimides with α-aminoalkyl radicals

1,3-Diamine synthesis: a new radical addition/acyl migration cascade process was reported, giving access to 1,3-diamines via photocatalyzed reactions of enamides with α-aminoalkyl radicals.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00239g
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Expedient access to α-(hetero)aryl-α-keto-1,3-diamines via redox-neutral photocatalyzed reactions of N-vinylimides with α-aminoalkyl radicals

Li Qiu, Yutao Jing, Yewen Fang, Yu Zhao et al.
1 citations
Organic Chemistry Frontiers
Radical Photochemical Reactions
0.94
article

Expedient access to α-(hetero)aryl-α-keto-1,3-diamines via redox-neutral photocatalyzed reactions of N-vinylimides with α-aminoalkyl radicals

Li Qiu, Yutao Jing, Yewen Fang, Yu Zhao, Yan Li
article en
1 citations

Abstract

1,3-Diamine synthesis: a new radical addition/acyl migration cascade process was reported, giving access to 1,3-diamines via photocatalyzed reactions of enamides with α-aminoalkyl radicals.

Organic Chemistry FrontiersVol. 12(13)
Ningbo University of Technology (CN), Tianjin University (CN), Ministry of Education (IR), Hubei University (CN), Taiyuan University of Technology (CN)
Openalex Percentile: Top 28%
Radical Photochemical Reactions
0.94
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