Rearrangement of 11-Hydroxy-11-(2-naphthyl)-3,4:8,9-dibenzobicyclo [4.4.1]undeca-3,8-diene-2,2,5,5,7,7,10,10-d_8

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Abstract

The preparation of a novel deuterated [3.3]orthocyclophane-alcohol is described. The rearrangement of the orthocyclophane alcohol leads to a dibenzo-annelated bromomethyldecaline. The deuterium labels provide a good indication of the mechanism that is underlying this reaction.

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