Reaction of BeCl2 with the dilithium diamide, [{SiNDipp}Li2] ({SiNDipp} = {CH2SiMe2NDipp}2), provides the dimeric chloroberyllate, [{SiNDippBeCl}Li]2, en route to the 2-coordinate beryllium amide, [SiNDippBe]. Lithium or sodium reduction of [SiNDippBe] in benzene, provides the relevant organoberyllate products, [{SiNDippBePh}M] (M = Li or Na), via the presumed intermediacy of transient Be(i) radicals.
CITATION STYLE
Pearce, K. G., Hill, M. S., & Mahon, M. F. (2023). Beryllium-centred C-H activation of benzene. Chemical Communications, 59(11), 1453–1456. https://doi.org/10.1039/d2cc06702a
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