Issue 7, 1986

Spontaneous resolution of an axially dissymmetric 3-carbamoylpyridinium iodide; intrinsic discrimination between the enantiomeric forms by the introduction of a second chiral element

Abstract

The direction of the carbonyl-orientation in a solid amide-rotamer of 3-[N-methyl-N-(R)-α-methylbenzyl]carbamoly-1,2,4-trimethylpyridinium iodide is governed by the (R)-chirality in the amide side chain; structures, as determined by X-ray analysis and c.d. spectra, are correlated.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 536-537

Spontaneous resolution of an axially dissymmetric 3-carbamoylpyridinium iodide; intrinsic discrimination between the enantiomeric forms by the introduction of a second chiral element

L. A. M. Bastiaansen, J. A. Kanters, F. H. van der Steen, J. A. C. de Graaf and H. M. Buck, J. Chem. Soc., Chem. Commun., 1986, 536 DOI: 10.1039/C39860000536

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