Quinoline Hydroxyalkylations from Iron-Catalyzed, Visible-Light-Driven Decarboxylations

One of the current challenges in organic synthesis is the direct alkylation of heterocyclic systems with a minimal impact on the environment. In this report, 4-substituted hydroxyalkyl quinolines were obtained by treating quinoline with different alkyl carboxylic acids in the presence of catalytic amounts of an iron (III) chloride–phenanthroline complex. The reaction was mediated by blue LED light under acidic conditions as a cleaner alternative to conventional heating, reducing the use of harmful substances.

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Publication Details

Journal
Catalysts
Published
2024-12-12
DOI
https://doi.org/10.3390/catal14120916
Citations
2
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.50
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article

Quinoline Hydroxyalkylations from Iron-Catalyzed, Visible-Light-Driven Decarboxylations

Erick Cuevas‐Yáñez, Nelly González‐Rivas, Zita G. Ríos-Malváez
2 citations
Catalysts
Radical Photochemical Reactions
0.50
article

Quinoline Hydroxyalkylations from Iron-Catalyzed, Visible-Light-Driven Decarboxylations

Erick Cuevas‐Yáñez, Nelly González‐Rivas, Zita G. Ríos-Malváez
article en
2 citations

Abstract

One of the current challenges in organic synthesis is the direct alkylation of heterocyclic systems with a minimal impact on the environment. In this report, 4-substituted hydroxyalkyl quinolines were obtained by treating quinoline with different alkyl carboxylic acids in the presence of catalytic amounts of an iron (III) chloride–phenanthroline complex. The reaction was mediated by blue LED light under acidic conditions as a cleaner alternative to conventional heating, reducing the use of harmful substances.

CatalystsVol. 14(12)
Universidad Autónoma del Estado de México (MX)
Openalex Percentile: Top 37%
Radical Photochemical Reactions
0.50
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