Iodine Enabled Mild 1,3-Hydroxyiodation of Arylcyclopropanes

1,3-difunctionalized skeletons are important feedstocks and frequently appear in pharmaceuticals. However, effective and straightforward approaches to these scaffolds remain challenging. Herein, we reported a mild and efficient strategy for 1,3-hydroxyiodation, employing molecular iodine as both the promoter and iodinating agent. This approach features mild conditions, good regio- and chemo-selectivity, high functional group tolerance, and easy derivatization of the products.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-09-09
DOI
https://doi.org/10.1021/acs.joc.5c01503
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
1.87
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article

Iodine Enabled Mild 1,3-Hydroxyiodation of Arylcyclopropanes

Zunli Lu, Wanrong Dong, Wen‐Ting Wei, Chunlan Song et al.
2 citations
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
1.87
article

Iodine Enabled Mild 1,3-Hydroxyiodation of Arylcyclopropanes

Zunli Lu, Wanrong Dong, Wen‐Ting Wei, Chunlan Song, Jiaxin Ai, Ting Guang
article en
2 citations

Abstract

1,3-difunctionalized skeletons are important feedstocks and frequently appear in pharmaceuticals. However, effective and straightforward approaches to these scaffolds remain challenging. Herein, we reported a mild and efficient strategy for 1,3-hydroxyiodation, employing molecular iodine as both the promoter and iodinating agent. This approach features mild conditions, good regio- and chemo-selectivity, high functional group tolerance, and easy derivatization of the products.

The Journal of Organic ChemistryVol. 90(37)
Hunan University (CN)
Openalex Percentile: Top 14%
Cyclopropane Reaction Mechanisms
1.87
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