Author:
Hartshorn MP,Penfold BR,Sutton KH,Vaughan J
Abstract
Reaction of
4-t-butyl-2,6-dimethylphenol (13) with nitrogen dioxide in cyclohexane proceeds
with some nitro-de-t-butylation, but reaction in benzene yields the four
possible 2,5,6-trinitrocyclohex- 3-enones (18), (19), (20), (21) and the
hydroxy dinitro ketone (22). The structures and stereochemistry of these
products were determined by single-crystal X-ray analysis. The mechanistic
significance of the formation of these trinitro ketones (18)-(21) is discussed.
Cited by
14 articles.
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