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- W2063985700 abstract "In the presence of AlBr3 in CS2 at temperatures below 0°, syn-tricyclo[4.2.1.12,5]decane (1) isomerizes exclusively to anti-tricyclo[4.2.1.12,5]decane (2) at a higher rate than the latter rearranges to 2-exo,3-exo-trimethylene-8,9,10-trinorbornane (4). However, at temperature above 0°, the anti-isomer 2 isomerizes to 4 faster than 1 to 2 and 4. As a consequence, hydride abstraction occurs at C(3) (→carbocation a, which rearranges to carbocation b (anti-skeleton)) in the syn-isomer 1, and more readily at C(9) (→carbocation c) than at C(3) (→carbocation b) in the anti-isomer 2." @default.
- W2063985700 created "2016-06-24" @default.
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- W2063985700 date "1987-11-04" @default.
- W2063985700 modified "2023-09-27" @default.
- W2063985700 title "The Aluminum-Bromide-Catalyzed Adamantane Rearrangement ofsyn- andanti-Tricyclo[4.2.1.12,5]decane" @default.
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- W2063985700 doi "https://doi.org/10.1002/hlca.19870700731" @default.
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