An Efficient Borafluorene for the Construction of Extended π-Conjugated Systems
Fukushima, Shoji and coworkers reported that 9-chloro-9-borafluorene mediates sequential alkyne insertion (1,2-carboboration) and oxidative deborylation/Csp2–Csp2 coupling reactions, affording extended π-conjugated molecules. The sequential reactions can be performed in a one-pot fashion and are very useful for the construction of a wide variety of π"-conjugated systems, which are potentially applicable to organic electronics.
References
- Boron-mediated sequential alkyne insertion and C–C coupling reactions affording extended π-conjugated molecules
- Y. Shoji, N. Tanaka, S. Muranaka, N. Shigeno, H. Sugiyama, K. Takenouchi, F. Hajjaj, T. Fukushima, Nat. Commun. 2016, 7, 12704.
