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Chemistry and Structure of Diterpene Compounds of the Kaurane Series: IV.1 Acylation of Reduction Products of the Isosteviol Keto Group
Authors:Al'fonsov  V. A.  Bakaleinik  G. A.  Gubaidullin  A. T.  Kataev  V. E.  Kovylyaeva  G. I.  Konovalov  A. I.  Litvinov  I. A.  Strobykina  I. Yu.  Andreeva  O. V.  Korochkina  M. G.
Affiliation:(1) Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center, Russian Academy of Sciences, Kazan, Tatarstan, Russia
Abstract:Acetylation with acetic anhydride of (4agr,8beta,13beta)-16-hydroxy-13-methyl-17-norkaurane-18-carboxylic acid and its methyl ester, obtained by reduction of isosteviol and (4agr,8beta,13beta)-18-methoxycarbonyl-13-methyl-16-oxo-17-norkaurane, respectively, gives rise to (4agr,8beta,13beta)-16-acetoxy-13-methyl-17-norkaurane-18-carboxylic acid and (4agr,8beta,13beta)-16-acetoxy-18-methoxycarbonyl-13-methyl-17-norkaurane. The molecular and crystal structures of the compounds were established by X-ray diffraction.
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