Pyrene-Based Organic Photoredox Catalysts for Carbon–Carbon Bond-Forming Reactions: Reductive Coupling of Aromatic Carbonyl and Imine Compounds

Metal-free photoredox catalysts built upon a pyrene core were developed for carbon-carbon bond-forming reactions. Among these catalysts, a pyrene derivative containing a urea moiety effectively facilitated the reductive coupling of aromatic carbonyl and imine compounds under blue LED irradiation. This process provided the corresponding vicinal diols and diamines in good yields.

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Publication Details

Journal
Organic Letters
Published
2024-09-05
DOI
https://doi.org/10.1021/acs.orglett.4c02845
Citations
5
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.25

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article

Pyrene-Based Organic Photoredox Catalysts for Carbon–Carbon Bond-Forming Reactions: Reductive Coupling of Aromatic Carbonyl and Imine Compounds

Shusuke Okamoto, Daisuke Nagai
5 citations
Organic Letters
Radical Photochemical Reactions
1.25
article

Pyrene-Based Organic Photoredox Catalysts for Carbon–Carbon Bond-Forming Reactions: Reductive Coupling of Aromatic Carbonyl and Imine Compounds

Shusuke Okamoto, Daisuke Nagai
article en
5 citations

Abstract

Metal-free photoredox catalysts built upon a pyrene core were developed for carbon-carbon bond-forming reactions. Among these catalysts, a pyrene derivative containing a urea moiety effectively facilitated the reductive coupling of aromatic carbonyl and imine compounds under blue LED irradiation. This process provided the corresponding vicinal diols and diamines in good yields.

Organic LettersVol. 26(36)
University of Shizuoka (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 23%
Radical Photochemical Reactions
1.25
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