Bromination of Cyclic 1, 3-Diketone Monoenolates with N-Bromosuccinimide. III.

Abstract

The position of substituted bromine in the product obtained by bromination with N-bromosuccinimide of 1, 3-cyclohexanedione 3-monoenolates having two alkyl substituents at the 5-position was established as 6, probably in axial conformation.