Biologically interesting fused oligocyclic lactams have been prepared via an intramolecular redox-neutral cyclization process. By the proper choice of the substrates with a wide variety of tethered olefins, the less favored C-H bond can be activated and functionalized. This C-H activation proceeds under mild conditions, obviates the need for external oxidants, and displays a broad scope with respect to the substituents. © 2014 Royal Society of Chemistry.
CITATION STYLE
Shi, Z., Boultadakis-Arapinis, M., Koester, D. C., & Glorius, F. (2014). Rh(iii)-Catalyzed intramolecular redox-neutral cyclization of alkenes via C-H activation. Chemical Communications, 50(20), 2650–2652. https://doi.org/10.1039/c4cc00029c
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