Heterodimers of Aromadendrane Sesquiterpenoid with Benzoquinone from the Chinese Liverwort Mylia nuda

Mylnudones A–G (1–7), unprecedented 1,10-seco-aromadendrane-benzoquinone-type heterodimers, and a highly rearranged aromadendrane-type sesquiterpenoid (8), along with four known analogs (9–12), were isolated from the liverwort Mylia nuda. Compounds 1–6 and 7, bearing tricyclo­[6.2.1.02,7] undecane and tricyclo­[5.3.1.02,6] undecane backbones, likely formed via a Diels–Alder reaction and radical cyclization, respectively. Their structures were determined by spectroscopic analysis, computational calculation, and single-crystal X-ray diffraction analysis. Dimeric compounds displayed cytoprotective effects against glutamic acid-induced neurological deficits.