Issue 5, 2004
From the journal:

Mendeleev Communications

Oxidation of betulin and its acetates with dimethyldioxirane

Olga Yu. Ashavina,a   Nataliya N. Kabalnova,a   Oxana B. Flekhter,a   Leonid V. Spirikhin,a   Fanur Z. Galin,a   Lidiya A. Baltina,a   Zoya A. Starikova,b   Mikhail Yu. Antipinb  and  Genrikh A. Tolstikovc  

a Institute of Organic Chemistry, Ufa Scientific Centre of the Russian Academy of Sciences, Ufa, Russian Federation, prosp. Oktyabrya 71, Ufa, Russian Federation

b A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, Russian Federation, ul. Vavilova, 28, Moscow, Russian Federation

c N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation, Prospekt Akademika Lavrent'eva, 9, Novosibirsk, Russian Federation

Abstract

The stereospecificity of epoxidation and the chemoselectivity of oxidation of hydroxy groups in the reactions of 20,29-lupene triterpenoids with dimethyldioxirane is discovered.

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Article information

DOI
https://doi.org/10.1070/MC2004v014n05ABEH001873
Article type
Communication
Submitted
08 Dec 2003

Mendeleev Commun., 2004,14, 221-223

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Oxidation of betulin and its acetates with dimethyldioxirane

O. Yu. Ashavina, N. N. Kabalnova, O. B. Flekhter, L. V. Spirikhin, F. Z. Galin, L. A. Baltina, Z. A. Starikova, M. Yu. Antipin and G. A. Tolstikov, Mendeleev Commun., 2004, 14, 221 DOI: 10.1070/MC2004v014n05ABEH001873

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