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- W2952543764 abstract "Abstract As a result of the fusion with five-membered oxygen rings, 2.3.6.7-tetrahydro- 2,2,4,6,6,8-hexamethylbenzo[1,2- b ;4,5- b ′]difuran ( 2a ) readily forms a cation radical ( 3 ), characterized as the tribromide and the hexachloroantimonate, that is halogenated by bromine or N-bromsuccinimide at any of the benzylic positions but with some preference for the ring methylene groups; the halogen in the products is so labile, however, that workup affords as the main product (33%) the 3,7-dione ( 4a )." @default.
- W2952543764 created "2019-06-27" @default.
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- W2952543764 date "1989-01-31" @default.
- W2952543764 modified "2023-09-23" @default.
- W2952543764 title "ChemInform Abstract: Bromination of the Cation Radical from a Derivative of 2,3,6,7-Tetrahydrobenzo(1,2-b;4,5-b′)difuran." @default.
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- W2952543764 doi "https://doi.org/10.1002/chin.198905102" @default.
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