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2.4.6.6 Variation 6: Via Ring Expansion Rearrangements

DOI: 10.1055/sos-SD-002-00214

Kündig, E. P.; Pache, S. H.Science of Synthesis, (20032187.

Tricarbonylchromium(0) complexes of benzocyclobutenone and benzocyclobutenedione can undergo ring expansion reactions leading to substituted tetraol (see Section 2.4.6.5), naphthol, benzocycloheptenedione, and annulated indanone complexes.[‌189‌,‌373‌] The naphthol complexes shown are the products of an alkoxy anion accelerated vinylcyclobutene cyclohexadiene rearrangement and benzocyclooctenedione complexes originate from a dianionic oxy-Copy rearrangement (Scheme 35).

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