Base-Dependent Divergent Carbodifluoroalkylation and Halodifluoroalkylation of Alkenes under Visible-Light Irradiation

Organic molecules containing a difluoroalkyl group are valuable and versatile chemicals because of their unique physicochemical and biological properties. Accordingly, the development of efficient and practical difluoroalkylation for the preparation of these compounds is important and attractive. Herein, we demonstrate photoredox-catalyzed and base-dependent selective carbodifluoroalkylation and halodifluoroalkylation of alkenes using readily available 2-(allyloxy)arylaldehydes [or 2-(allylamino)arylaldehydes] and XCF<sub>2</sub>COOEt (or BrCF<sub>2</sub>CONR<sup>1</sup>R<sup>2</sup>) as starting materials. The developed reaction enables convenient and accurate synthesis of difluoroalkylated chroman-4-ones and aldehydes and features broad substrate scope, mild conditions, and operational simplicity. Moreover, gram-scale product preparation and application of the title protocol in late-stage functionalization of pharmaceutical molecules are accomplished.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-09-03
DOI
https://doi.org/10.1021/acs.joc.4c01591
Citations
6
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
1.25

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article

Base-Dependent Divergent Carbodifluoroalkylation and Halodifluoroalkylation of Alkenes under Visible-Light Irradiation

Qiuju Zhou, Lin Tang, Lufang Zhang, Fengjuan Jia et al.
6 citations
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
1.25
article

Base-Dependent Divergent Carbodifluoroalkylation and Halodifluoroalkylation of Alkenes under Visible-Light Irradiation

Qiuju Zhou, Lin Tang, Lufang Zhang, Fengjuan Jia, Lingyun Zheng, Taijun Wu, Xinmeng Wei
article en
6 citations

Abstract

Organic molecules containing a difluoroalkyl group are valuable and versatile chemicals because of their unique physicochemical and biological properties. Accordingly, the development of efficient and practical difluoroalkylation for the preparation of these compounds is important and attractive. Herein, we demonstrate photoredox-catalyzed and base-dependent selective carbodifluoroalkylation and halodifluoroalkylation of alkenes using readily available 2-(allyloxy)arylaldehydes [or 2-(allylamino)arylaldehydes] and XCF<sub>2</sub>COOEt (or BrCF<sub>2</sub>CONR<sup>1</sup>R<sup>2</sup>) as starting materials. The developed reaction enables convenient and accurate synthesis of difluoroalkylated chroman-4-ones and aldehydes and features broad substrate scope, mild conditions, and operational simplicity. Moreover, gram-scale product preparation and application of the title protocol in late-stage functionalization of pharmaceutical molecules are accomplished.

The Journal of Organic ChemistryVol. 89(18)
Xinyang Normal University (CN)
National Natural Science Foundation of China, Education Department of Henan Province, Nanhu Scholars Program for Young Scholars of Xinyang Normal University
Openalex Percentile: Top 23%
Fluorine in Organic Chemistry
1.25
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