Two series of mono-substituted N-benzylideneanilines, 1 and 2, have been synthesized. The substituents were placed in the C-phenyl ring and the N-phenyl ring at either the 3 or 4 positions. This is a report of preliminary results for substituent effects on 13C chemical shifts in both phenyl rings and at the benzylic carbon in deuterochloroform solution. The effects on the 1H chemical shifts for the methine proton will also be shown.
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Back to The 37th Middle Atlantic Regional Meeting (May 22-25, 2005)