Force field and multinuclear nmr study of the conformational properties of thiolane-1-oxide and its mono and dimethyl derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. Conformational analysis of the thiolane ring system. I. Stereochemistry of the base-catalyzed hydrogen-deuterium exchange, pyramidal inversion, and proton magnetic resonance spectrum of trans-3-methyl-3-thioniabicyclo[4.3.0]nonane iodide, a conformationally rigid thiolanium cation
2. Conformational analysis of the thiolane ring system. II. Proton magnetic resonance spectra and base-catalyzed hydrogen-deuterium exchange of sulfonium cations and sulfoxides derived from 3,3-dimethylthiolane and trans-2-thiahydrindan
3. 13C NMR of organosulphur compounds: I—the effects of sulphur substituents on the13C chemical shifts of alkyl chains and of S-heterocycles
4. 13C chemical shifts and conformational analysis of methyl substituted thiacyclopentanes
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