Indenone is made in two steps from indane-1,3-dione, and a by-product is characterised by conversion to s-dibenzofulvalene. Indenone undergoes acid-catalysed addition reactions, and all its six protons have magnetic resonance at higher field than expected.
P. H. Lacy and D. C. C. Smith, J. Chem. Soc. C, 1971, 41 DOI: 10.1039/J39710000041
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