Spontaneous resolution of an axially dissymmetric 3-carbamoylpyridinium iodide; intrinsic discrimination between the enantiomeric forms by the introduction of a second chiral element
- 1 January 1986
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 7,p. 536-537
- https://doi.org/10.1039/c39860000536
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.Keywords
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