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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1994 Volume 4, Issue 5, Page 172 (Mi mendc5203)

This article is cited in 3 papers

Synthesis of Cyclo-substituted Triangulanes with Four and Five Spiroannulated Three-membered Rings by Sequential Peripheral Cyclopropanation of Cyclooctene

T. S. Kuznetsovaa, O. V. Eremenkoa, O. V. Kokorevaa, G. V. Zatonskyb, N. S. Zefirova

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Synthesis of pentacyclo[9.1.0.01 3.03.5.05.7]dodecane 4 and hexacyclo[10.1.0.01 3.03.5.05.7.07.9]tridecane 5 has been performed, based on sequential bromocyclopropanation of the C=C bond and elimination to give a repeating endomethylenecyclopropane framework, with termination of the sequence by cyclopropanation.

Language: English

DOI: 10.1070/MC1994v004n05ABEH000399



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