Author:
Feutrill GI,Mirrington RN
Abstract
The synthesis of
3-(2?-hydroxyphenyl)-2,3-dimethylcyclopent-ene (8) has been effected in six
steps from o-iodoanisole; a key step was the conversion of (7) into (8), each
being acid-sensitive, by demethylation with sodium thioethoxide in dimethyl-formamide.
��� The reactions of (8) and its acetate (22)
with several methylenating agents were examined, but no cyclopropane-containing
products were obtained.
Cited by
9 articles.
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