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Chlorination of tectochrysin and pinostrobin in methanol
Authors:Kulmagambetova  E. A.  Seitembetova  A. G.  Kulyjasov  A. T.  Raldugin  V. A.  Gatilov  Yu. V.  Shakirov  M. M.  Adekenov  S. M.  Tolstikov  G. A.
Affiliation:(1) Ministry of Education and Sciences of the Republic of Kazakhstan, Institute of Phytochemistry, 4 ul. Gazalieva, 470032 Karaganda, Kazakhstan;(2) N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp. Akad. Lavrent"eva, 630090 Novosibirsk, Russian Federation
Abstract:The reactions of the natural flavonoids tectochrysin and pinostrobin with chlorine in methanol afforded for the first time their 6,8-dichloro derivatives. Under the reaction conditions, dichloropinostrobin was transformed further into a tetrachloromethoxy derivative. The molecular structure of the latter was established by X-ray diffraction analysis.
Keywords:flavonoids  tectochrysin  pinostrobin  chlorination  X-ray diffraction analysis  2D NMR spectroscopy
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