Refine
Has Fulltext
- yes (113)
Is part of the Bibliography
- yes (113)
Year of publication
Document Type
- Journal article (83)
- Preprint (30)
Keywords
- boron (46)
- diborenes (15)
- Boron (11)
- carbenes (9)
- inorganic chemistry (8)
- Bor (7)
- density functional calculations (6)
- diborynes (6)
- aromaticity (5)
- heterocycles (5)
Institute
Sonstige beteiligte Institutionen
Dihalodiboranes(4) react with an N-heterocyclic silylene (NHSi) to generate NHSi-adducts of 1-aryl-2-silyl-1,2-diboraindanes as confirmed by X-ray crystallography, featuring the functionalization of both B–X (X = halogen) bonds and a C–H bond under mild conditions. Coordination of a third NHSi to the proposed 1,1-diaryl- 2,2-disilyldiborane(4) intermediates, generated by a two-fold B–X insertion, may be crucial for the C–H borylation that leads to the final products. Notably, our results demonstrate the first C–H borylation with a strong B–F bond activated by silylene insertion.