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Nuclear magnetic resonance of chiral molecules. II. Intramolecular interactions in thiazolidinethiones

Journal Article · · J. Org. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:6388197
Thiazolidinethiones were investigated by the PMR method in order to compare the magnetically anisotropic characteristics of the acetylene and ethylene bonds and to study their conformation. A conformation with an intramolecular hydrogen bond, including the sulfur atom and the proton of the hydroxyl group, is proposed on the basis of an analysis of the factors affecting the chemical nonequivalence of the geminal methyl groups at the ..cap alpha.. position to the asymmetric carbon atom. The conformation clearly explains the characteristics of the PMR spectra of the thiazolidinethiones.
Research Organization:
V.I. Nikitin Institute of Chemistry, Dushanbe, USSR
OSTI ID:
6388197
Journal Information:
J. Org. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Org. Chem. USSR (Engl. Transl.); (United States) Vol. 22:5; ISSN JOCYA
Country of Publication:
United States
Language:
English

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