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Conformational difference between mono- and diprotonated cis-2,5-diphenylpiperazinium salts in the solid state
K Takasu1, H Miyamoto, K Tanaka
1Institute for Chemical Research, Kyoto University, Uji, Japan.
Chemical & Pharmaceutical Bulletin
|January 6, 2001
Abstract:
Monohydrochlorides of cis-2,5-diphenylpiperazine assume a chair conformation, while the corresponding dihydrochlorides assume a boat form regardless of the substituent(s) at the nitrogen atom.
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