Preparation of Vitamin K3 in Mo–V–P Heteropoly Acid Solutions by Diene Synthesis

The possibility of obtaining vitamin K 3 (2-methyl-1,4-naphthoquinone, menadione) by diene synthesis from accessible substrates such as 2-methylphenol ( o -cresol) and 2-methylaniline ( o -toluidine) was shown. The bifunctional catalysts of these processes are the aqueous solutions of Mo–V–P heterop...

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Veröffentlicht in:Kinetics and catalysis 2020, Vol.61 (2), p.276-282
Hauptverfasser: Gogin, L. L., Zhizhina, E. G.
Format: Artikel
Sprache:eng
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Zusammenfassung:The possibility of obtaining vitamin K 3 (2-methyl-1,4-naphthoquinone, menadione) by diene synthesis from accessible substrates such as 2-methylphenol ( o -cresol) and 2-methylaniline ( o -toluidine) was shown. The bifunctional catalysts of these processes are the aqueous solutions of Mo–V–P heteropoly acids, which allow the oxidation and diene synthesis to be performed as a one-pot process.
ISSN:0023-1584
1608-3210
DOI:10.1134/S0023158420010012