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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1998 Volume 8, Issue 6, Pages 233–236 (Mi mendc4744)

This article is cited in 4 papers

Reaction of N,N-dimethylaniline with 1,5-diferrocenyl-3-methyl-2,4-trimethylene-penta-1,4-dienyl carbocation. A nonsynchronous cationic cyclodimerization mechanism in conjugated dienes

E. I. Klimovaa, T. Klimova-Berestnevaa, M. Martinez Garciab, L. Ruiz-Ramireza

a Materials Research Institute, National Autonomous University of Mexico, Mexico, Mexico
b Institute of Chemistry, National Autonomous University of Mexico, Mexico, Mexico

Abstract: Reaction of the 1,5-diferrocenyl-3-methyl-2,4-trimethylenepenta-1,4-dienyl tetrafluoroborate cation with N,N-dimethylaniline affords a mixture of products from the alkylation of N,N-dimethylaniline at the para-position by monomeric and linear and cyclic dimeric carbocations along with linear and cyclic dimers of 1,3-diferrocenylmethylene-2-methylenecyclohexane. These results confirm and illustrate a nonsynchronous cationic cyclodimerization mechanism for ferrocenylbuta-1,3-dienes.

Language: English

DOI: 10.1070/MC1998v008n06ABEH001015



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