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In the title compound, C14H12O2, the cyclo­hexene ring adopts an envelope conformation, while the remaining fragment of the anthraquinone skeleton is planar.

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The title compound, C22H26BNO3, is the first example of a boron-containing enaminone to be characterized by X-ray diffraction. The B atom lies in a three-coordinate environment and shows no additional intra- or inter­molecular inter­actions. The 4,4,5,5-tetra­methyl-1,3,2-dioxaborolan-2-yl group is roughly coplanar with the adjacent aromatic ring, as expected if considerable dative bonding is occurring between the aromatic p-π electrons and the empty p-orbital on the B atom.
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