Spontaneous Resolution of an Axially Dissymmetric 3-Carbamoylpyridinium Iodide; Intrinsic Discrimination between the Enatiomeric Forms by the Introduction of a Second Chiral Element

DOI: 10.1039/c39860000536

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Journal of the Chemical Society. Chemical communications p. 536 - 537 (1986)

Update date:2022-07-30

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Authors:

Bastiaansen, Loek A. M.

Kanters, Jan A.

Steen, Fred H. van der

Graaf, John A. C. de

Buck, Henk M.

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Article abstract of DOI:10.1039/c39860000536

The direction of the carbonyl-orientation in a solid amide-rotamer of 3-carbamoyl-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

Full text of DOI:10.1039/c39860000536

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