Stereostructure of isomeric (±)-1-thioflavanone 1-oxides

A. Bényei, László Somogyi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

The synthesis, separation and stereochemistry of 1-epimeric (±)-1-thioflavanone 1-oxide isomers with equatorial phenyl group are described. The higher melting isomer (2a) has a l,2-cis-, the lower melting one (2b) a 1,2-trans configuration. 1H NMR and mass spectral data for both isomers and X-ray diffraction analysis of 2a are also presented.

Original languageEnglish
Pages (from-to)191-196
Number of pages6
JournalPhosphorus, Sulfur and Silicon and Related Elements
Volume143
Publication statusPublished - 1998

Fingerprint

Isomers
Oxides
Freezing
Melting
X-Ray Diffraction
Stereochemistry
X ray diffraction analysis
Nuclear magnetic resonance
thioflavanone
Proton Magnetic Resonance Spectroscopy

Keywords

  • Stereoisomerism
  • Sulfoxides
  • Thiopyrans
  • X-Ray crystallography

ASJC Scopus subject areas

  • Inorganic Chemistry

Cite this

Stereostructure of isomeric (±)-1-thioflavanone 1-oxides. / Bényei, A.; Somogyi, László.

In: Phosphorus, Sulfur and Silicon and Related Elements, Vol. 143, 1998, p. 191-196.

Research output: Contribution to journalArticle

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