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1H, 13C, 17O NMR and quantum-chemical study of the stereochemistry of the sulfoxide and sulfone derivatives of 3-arylidene-1-thioflavan-4-one epoxides

✍ Scribed by József Kovács; Gábor Tóth; András Simon; Albert Lévai; Andreas Koch; Erich Kleinpeter

Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
277 KB
Volume
41
Category
Article
ISSN
0749-1581

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✦ Synopsis

Abstract

The oxidation of the trans,cis‐(2) and trans,trans‐epoxides (3) of differently substituted (Z)‐3‐arylidene‐1‐thioflavan‐4‐ones (1) with dimethyldioxirane (DMD) yielded the appropriate sulfoxides (4, 5) and sulfones (6, 7). The structures were elucidated by the extensive application of one‐ and two‐dimensional ^1^H, ^13^C and ^17^O NMR spectroscopy. The conformational analysis was achieved by the application of ^3^J(C,H) coupling constants, NOESY responses and ab initio calculations. The preferred ground‐state conformers (twisted envelope‐A, twisted envelope‐B for 6 and twisted envelope‐A, envelope‐B for 7) were obtained as global minima of the theoretical ab initio MO study and also the examination of the ^17^O and ^13^C chemical shifts, calculated for the global minima structures of the sulfone isomers by the GIAO method. Analogous results, obtained for the sulfoxide isomers (4, 5), not only led to the preferred conformers but also gave evidence for the trans arrangement of the 2‐Ph group and the oxygen atom of the SO group. Chemical shift differences between the isomers, sulfoxides and sulfones were corroborated by ab initio calculations of the anisotropic effects of the oxirane ring and the SO and SO~2~ groups. Copyright © 2003 John Wiley & Sons, Ltd.

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