Epoxidation of (Z)-3-arylidene-1-thioflavanones

A. Lévai, G. Tóth, J. Kovács, T. Patonay, E. B. Vass

Research output: Article

5 Citations (Scopus)

Abstract

Epoxidation of (Z)-3-arylidene-1-thioflavanones by sodium hypochlorite or alkaline hydrogen peroxide afforded diastereomeric mixtures of trans,cis- and trans,trans-epoxides. These were separated by silica gel column chromatography. Determination of the isomeric composition of the crude reaction products and structure elucidation of all new isolated epoxides were performed by 1H and 13C NMR spectroscopy.

Original languageEnglish
Pages (from-to)707-713
Number of pages7
JournalMonatshefte fur Chemie
Volume132
Issue number6
DOIs
Publication statusPublished - 2001

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Epoxidation
Epoxy Compounds
Sodium Hypochlorite
Column chromatography
Silica Gel
Reaction products
Hydrogen Peroxide
Nuclear magnetic resonance spectroscopy
Chemical analysis
thioflavanone

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Epoxidation of (Z)-3-arylidene-1-thioflavanones. / Lévai, A.; Tóth, G.; Kovács, J.; Patonay, T.; Vass, E. B.

In: Monatshefte fur Chemie, Vol. 132, No. 6, 2001, p. 707-713.

Research output: Article

Lévai, A. ; Tóth, G. ; Kovács, J. ; Patonay, T. ; Vass, E. B. / Epoxidation of (Z)-3-arylidene-1-thioflavanones. In: Monatshefte fur Chemie. 2001 ; Vol. 132, No. 6. pp. 707-713.
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