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Mendeleev Communications, 2007, Volume 17, Issue 3, Pages 170–171
DOI: https://doi.org/10.1016/j.mencom.2007.05.013 (Mi mendc3415) 		 
This article is cited in 5 scientific papers (total in 5 papers)

Facial selectivity in the reaction of dihalocarbenes with 2-substituted 4,7-dihydro-1,3-dioxepines

V. Yu. Fedorenko, R. N. Baryshnikov, R. M. Vafina, Yu. G. Shtyrlin, E. N. Klimovitskii

Alexander Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation
Full-text PDF (214 kB) Citations (5)
DOI: https://doi.org/10.1016/j.mencom.2007.05.013
Abstract: The dichloro(dibromo)cyclopropanation of conformationally heterogeneous 2-substituted 4,7-dihydro-1,3-dioxepines was found to afford a low selectivity; endo addition on the side of a remote alkyl substitutent is governed by the π-facial solvation of substrates.
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Document Type: Article
Language: English


Citation: V. Yu. Fedorenko, R. N. Baryshnikov, R. M. Vafina, Yu. G. Shtyrlin, E. N. Klimovitskii, “Facial selectivity in the reaction of dihalocarbenes with 2-substituted 4,7-dihydro-1,3-dioxepines”, Mendeleev Commun., 17:3 (2007), 170–171
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  • https://www.mathnet.ru/eng/mendc/v17/i3/p170
    • This publication is cited in the following 5 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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