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.
Authors
- Zunli Lu (ORCID: https://orcid.org/0000-0003-4250-3178)
- Wanrong Dong (ORCID: https://orcid.org/0000-0002-6541-2853)
- Wen‐Ting Wei (ORCID: https://orcid.org/0000-0001-7942-8656)
- Chunlan Song (ORCID: https://orcid.org/0000-0002-8750-9306)
- Jiaxin Ai
- Ting Guang
Institutions
- Hunan University (CN)
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