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- W2952742356 abstract "Convenient new preparations of 1-halogeno-1,2-dihydrobenzocyclobutenes (5) and (6) and 1,1′-bi(benzocyclobutylidene)(4) are described. The hydrocarbon (4) is susceptible to cationic rearrangements: it forms 5,10-dihydroindeno[2,1-a]indene (16) on protonation in acetic anhydride, and is oxidised by selenium(IV) oxide to a mixture of the spiroketone (17) and 5H-indeno[1,2-c]-[2]benzopyran-2-one (18). The mechanisms of these and other rearrangements are discussed." @default.
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- W2952742356 date "1987-11-03" @default.
- W2952742356 modified "2023-09-27" @default.
- W2952742356 title "ChemInform Abstract: Synthesis and Rearrangements of 1,1′-Bi(benzocyclobutylidene) and Its Derivatives." @default.
- W2952742356 cites W2171640654 @default.
- W2952742356 doi "https://doi.org/10.1002/chin.198744152" @default.
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