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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2015 Volume 25, Issue 6, Pages 449–451 (Mi mendc2441)

This article is cited in 9 papers

Communications

Stereoselective synthesis of spirocyclic nitronates by SnCl4-promoted reaction of nitroalkenes with C-2 substituted 4-methylidene-1,3-dioxolane

A. A. Mikhaylov, P. A. Zhmurov, A. S. Naumova, Yu. A. Khoroshutina, A. Yu. Sukhorukov, S. L. Ioffe

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: SnCl4-promoted [4 + 2] cycloaddition of β-nitrostyrenes to 4-methylidene-1,3-dioxolane provides stereoselective synthesis of spirocyclic nitronates. 2-Nitrovinyl benzoate under the same conditions produces δ-substituted nitrodiene as a single E,E-isomer.

Language: English

DOI: 10.1016/j.mencom.2015.11.017



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