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Mendeleev Communications, 2004, Volume 14, Issue 6, Pages 299–301
DOI: https://doi.org/10.1070/MC2004v014n06ABEH002061
(Mi mendc3919)
 

This article is cited in 12 scientific papers (total in 12 papers)

Generation and stereocontrolled trapping of 3-phenylcyclopropene and its derivatives

A. E. Shesheneva, M. S. Bairdb, A. K. Croftb, I. G. Bolesova

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b Department of Chemistry, University of Wales, Bangor, UK
Abstract: Selective methods for the preparation of 3-phenylcyclopropene and its 1-substituted derivatives are provided. The parent cyclopropene is readily trapped in (3+2)- and (4+2)-cycloadditions that lead to exo-3-phenyl-1,2-disubstituted cyclopropanes. Ab initio calculations suggest that the lowest energy conformation has the plane of the benzene ring perpendicular to the cyclopropene π-bond but with a low rotation barrier.
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Document Type: Article
Language: English


Citation: A. E. Sheshenev, M. S. Baird, A. K. Croft, I. G. Bolesov, “Generation and stereocontrolled trapping of 3-phenylcyclopropene and its derivatives”, Mendeleev Commun., 14:6 (2004), 299–301
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  • https://www.mathnet.ru/eng/mendc/v14/i6/p299
  • This publication is cited in the following 12 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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