Photomediated Radical Cascade Addition–Cyclization of N-Butenoyl Tetrahydroquinolines: Accessing Functionalized Julolidines

Herein, we describe the photomediated radical cascade addition-cyclization of N-butenoyl tetrahydroquinolines to access various functionalized julolidine-5-one. The scope of the methodology was illustrated with several sulfonyl chlorides and tetrahydroquinolines. Other radical precursors, such as trifluoromethyl, bromoacetonitrile, bromoacetates, etc., also worked efficiently, demonstrating the broad utility of the method. Finally, large-scale synthesis of sulfonyl-substituted julolidine-5-one and downstream conversions of the synthesized julolidine derivatives were carried out to illustrate the synthetic utility of the methodology.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-14
DOI
https://doi.org/10.1021/acs.joc.5c00234
Citations
2
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Photomediated Radical Cascade Addition–Cyclization of N-Butenoyl Tetrahydroquinolines: Accessing Functionalized Julolidines

Purushothaman Gopinath, Burkhard Koenig, Naremaddepalli S. Sudarshan, Ajal P. Shaji
2 citations
The Journal of Organic Chemistry
Radical Photochemical Reactions
1.87
article

Photomediated Radical Cascade Addition–Cyclization of N-Butenoyl Tetrahydroquinolines: Accessing Functionalized Julolidines

Purushothaman Gopinath, Burkhard Koenig, Naremaddepalli S. Sudarshan, Ajal P. Shaji
article en
2 citations

Abstract

Herein, we describe the photomediated radical cascade addition-cyclization of N-butenoyl tetrahydroquinolines to access various functionalized julolidine-5-one. The scope of the methodology was illustrated with several sulfonyl chlorides and tetrahydroquinolines. Other radical precursors, such as trifluoromethyl, bromoacetonitrile, bromoacetates, etc., also worked efficiently, demonstrating the broad utility of the method. Finally, large-scale synthesis of sulfonyl-substituted julolidine-5-one and downstream conversions of the synthesized julolidine derivatives were carried out to illustrate the synthetic utility of the methodology.

The Journal of Organic ChemistryVol. 90(16)
Indian Institute of Science Education and Research, Tirupati (IN), University of Regensburg (DE)
Alexander von Humboldt-Stiftung
Openalex Percentile: Top 16%
Radical Photochemical Reactions
1.87
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