Iron-Catalyzed\nMiyaura Borylation of Aryl Chlorides\nand Triflates
Simple aryl chlorides represent challenging substrates\nin iron-catalyzed\nborylation. A combination of Li[B(<sup>t</sup>Bu)pin-Bpin] as the\nborylating reagent and a catalyst formed in situ from iron(II) triflate\nand the commercially available N-heterocyclic carbene ligand, IMes,\ngives significantly improved activity and a much broader scope than\npreviously reported iron-based catalysts. Iron triflate is also a\ngood precatalyst for the borylation of aryl triflatesa previously\nunreported transformationand in these cases the IMes ligand\nis not required.
Publication Details
- Journal
- Figshare
- Published
- 2024-12-17
- DOI
- https://doi.org/10.1021/acs.orglett.4c04171.s001
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00