Abstract
α,α?-Dibromocycloalkanones react with organoboranes
in the presence of base to give products dependent on the amount and type of
base used. Small alkoxides yield mainly the reduced cycloalkanone; one equivalent of more hindered alkoxides also leads to reduction, but two equivalents of
hindered alkoxides afford monoalkylcycloalkanones.
Unsymmetrical dibromo ketones give alkylation
exclusively on the least hindered side.
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