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Conformational preference and configurational control of highly symmetric spirobi[dibenzazepinium] cation
1Département de Chimie Organique, Université de Genève, quai Ernest-Ansermet 30, CH-1211 Genève 4, Switzerland.
Organic Letters
|February 26, 2003
Abstract:
[formula: see text] Stereodynamics were detected in solution for salts of the simple spirobi[dibenzazepinium] cation in favor of the homochiral (D2) conformer as evidenced by chiral TRISPHAT and BINPHAT counterions; asymmetric induction was furthermore observed in 1H and 15N NMR spectroscopy.