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Mendeleev Communications, 2013, Volume 23, Issue 2, Pages 92–93
DOI: https://doi.org/10.1016/j.mencom.2013.03.013
(Mi mendc2625)
 

This article is cited in 27 scientific papers (total in 27 papers)

Friedel–Crafts alkylation of natural amino acid-derived pyrroles with CF3-substituted cyclic imines

O. I. Shmatovaa, N. E. Shevchenkoa, E. S. Balenkovaa, G.-V. Roeschenthalerb, V. G. Nenajdenkoa

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b School of Engineering and Science, Jacobs University of Bremen, Bremen, Germany
Abstract: Natural amino acid-derived ethyl 2-(1-pyrrolyl)alkanoates react with 2-trifluoromethyl-1-azacycloalkenes selectivity at the b-position of the pyrrole moiety to afford ethyl 2-[3-(1-trifluoromethyl-2-azacycloalkyl)pyrrol-1-yl]alkanoates.
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Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (441.9 Kb)


Citation: O. I. Shmatova, N. E. Shevchenko, E. S. Balenkova, G.-V. Roeschenthaler, V. G. Nenajdenko, “Friedel–Crafts alkylation of natural amino acid-derived pyrroles with CF3-substituted cyclic imines”, Mendeleev Commun., 23:2 (2013), 92–93
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  • https://www.mathnet.ru/eng/mendc/v23/i2/p92
  • This publication is cited in the following 27 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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