Abstract
Versatile C–H amidations of synthetically useful ferrocenes were accomplished by weakly-coordinating thiocarbonyl-assisted cobalt catalysis. Thus, carboxylates enabled ferrocene C–H nitrogenations with dioxazolones, featuring ample substrate scope and robust functional group tolerance. Mechanistic studies provided strong support for a facile organometallic C–H activation manifold.
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Yetra, S. R., Shen, Z., Wang, H., & Ackermann, L. (2018). Thiocarbonyl-enabled ferrocene C–H nitrogenation by cobalt(III) catalysis: Thermal and mechanochemical. Beilstein Journal of Organic Chemistry, 14, 1546–1553. https://doi.org/10.3762/bjoc.14.131
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