Abstract
Abstract A series of N -substituted-9-phenethyl-3-amino norgranatane derivatives have been synthesized and studied by 1 H and 13 C NMR spectroscopy. The compounds studied display in deuterochloroform the same preferred flattened chair-boat conformation with the disubstituted ring in a slightly distorted boat form. The arylamino groups, in the C-3α position lie in the symmetry plane with respect to the bicyclic system.
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