Recent advances in haloarene synthesis by aryne reactions
<h2>Abstract</h2> Recent advances in haloarene synthesis by diverse transformations of aryne intermediates are summarized in this review. Regioselective reactions of 3-haloaryne intermediates have enabled the efficient synthesis of a wide variety of haloarenes, facilitated by structural distortion induced by the electron-withdrawing nature of halogen substituents. In addition, numerous halogenation-based transformations of aryne intermediates have been developed for the construction of highly functionalized haloarenes. These innovative aryne-based strategies offer access to structurally unique aromatic compounds, highlighting the pivotal role of halogens in modern synthetic chemistry. As a result, emerging synthetic methods involving aryne intermediates have proven valuable in various research fields, including materials chemistry and pharmaceutical sciences.
Authors
- Suguru Yoshida (ORCID: https://orcid.org/0000-0001-5888-9330)
- Shinya Tabata
Institutions
- Tokyo University of Science (JP)
Publication Details
- Journal
- Tetrahedron Chem
- Published
- 2025-05-30
- DOI
- https://doi.org/10.1016/j.tchem.2025.100136
- Primary Topic
- Cyclization and Aryne Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Society for the Promotion of Science