Divergent Synthesis of Silacycles by Ligand-Controlled Rhodium-Catalyzed Annulation of (2-Hydrosilylaryl)acetylenes
This study demonstrates the rhodium-catalyzed divergent synthesis of 5-, 5,6-, and 8-membered silacyclic compounds, such as benzosilole, silolosiline, and disilocine, from (2-hydrosilylaryl)acetylenes. To achieve high product selectivity, intra- and intermolecular reactions are controlled by tuning the mono- and bidentate phosphine ligands on the rhodium catalyst precursor. Deuterium labeling experiments and computational studies reveal that the annulation reaction proceeds via hydride transfer to the alkyne moiety.
Authors
- Kyohei Kawashima (ORCID: https://orcid.org/0000-0002-9335-8145)
- Kazuto Fuji
- Yoichiro Kuninobu (ORCID: https://orcid.org/0000-0002-8679-9487)
- Toshifumi Mori (ORCID: https://orcid.org/0000-0003-0188-0794)
- Kohei Sekine (ORCID: https://orcid.org/0000-0001-7588-3176)
Institutions
- Kyushu University (JP)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-02-06
- DOI
- https://doi.org/10.1021/acs.orglett.4c04694
- Citations
- 2
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- Shorai Foundation for Science and Technology
- Tokuyama Science Foundation
- Japan Society for the Promotion of Science