Abstract
The structures assigned to the 4-aminocyclohexanols
have been confirmed and some fundamental reactions studied. Solvolysis of
trans-4-benzamidocyclohexyl toluene-p-sulphonate has shown absence of
participation in the rate-determining step although product analysis indicates
that the reaction proceeds with retention of configuration. The bromination of
4-benzamidocyclohexene and solvolysis of the products have been studied.
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10 articles.
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