Allylic inversion of the migrating group in the acid-catalysed rearrangement of a 2,6-di-t-butylcyclohexa-2,5-dienone
Abstract
The acid-catalysed migration of an allyl group from C-4 to C-2 of a 2,6-di-t-butylcyclohexa-2,5-dienone proceeds with essentially complete allylic inversion, while migration to C-3 proceeds without inversion.
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