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- W2086021910 abstract "The bromination of 3-bromo-6,7-benzobicyclo [3.2.1] octa-2,6-diene at -50°C has been found to give only one product, the tribromide 8 produced via Wagner-Meerwein rearrangement with accompanying aryl migration. The bromination at 0°C produced nonrearranged tribromides beside the rearranged tribromide and the ketone 12. The structures of the products were determined by 1H-, 13C-NMR data and single X-ray structural analysis. The addition mechanism is discussed in terms of exo- and endo-attack." @default.
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- W2086021910 date "1988-01-01" @default.
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- W2086021910 title "The Bromination of 3-Bromo-6,7-benzobicyclo [3,2,1] octa-2,6-diene and characterization of the products" @default.
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- W2086021910 doi "https://doi.org/10.1016/s0040-4020(01)85995-0" @default.
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