Abstract
AbstractA cyclopropyl cation, stabilized by a p‐anisyl groupAnisyl = methoxyphenyl. , turns out to be an intermediate in the alcoholysis of 1‐(p‐anisyl)cyclopropyl halides. In other reactions with nucleophiles substitution products are also formed predominantly without ring rupture.The influence of the solvent, nature of nucleophiles and added salts on reaction rates and product distributions support an SN1 type mechanism.
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