An Efficient Synthesis of Aromatic Aldehydes by Iron-Catalyzed Reductive Carbonylation of Aryl Iodides

Reductive carbonylation of aryl halides (Hlg = Cl, Br, I) by using carbon monoxide as carbonyl source in the presence of iron catalyst, silyl hydride, and base under mild reaction conditions afforded the corresponding aromatic aldehydes. In this methodology, aryl iodides were conveniently transformed to aldehydes in moderate to excellent yields.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2024-10-01
DOI
https://doi.org/10.1134/s1070428024100233
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.50
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article

An Efficient Synthesis of Aromatic Aldehydes by Iron-Catalyzed Reductive Carbonylation of Aryl Iodides

Rajesh Akkineni, Venkateswara Rao Battula, Kalidasu Sheelam, S. Paul Douglas
2 citations
Russian Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.50
article

An Efficient Synthesis of Aromatic Aldehydes by Iron-Catalyzed Reductive Carbonylation of Aryl Iodides

Rajesh Akkineni, Venkateswara Rao Battula, Kalidasu Sheelam, S. Paul Douglas
article en
2 citations

Abstract

Reductive carbonylation of aryl halides (Hlg = Cl, Br, I) by using carbon monoxide as carbonyl source in the presence of iron catalyst, silyl hydride, and base under mild reaction conditions afforded the corresponding aromatic aldehydes. In this methodology, aryl iodides were conveniently transformed to aldehydes in moderate to excellent yields.

Russian Journal of Organic ChemistryVol. 60(10)
Andhra University (IN)
Openalex Percentile: Top 37%
Catalytic C–H Functionalization Methods
0.50
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