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Mendeleev Communications, 2015, Volume 25, Issue 6, Pages 438–439
DOI: https://doi.org/10.1016/j.mencom.2015.11.013
(Mi mendc2437)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

Lewis acid-catalyzed reactions of N-allylanilines with diazo compounds involving aza-Claisen rearrangement

A. G. Badamshinab, L. V. Spirikhinb, R. F. Salikovc, V. A. Dokichevab, Yu. V. Tomilovc

a Institute of Physics of Advanced Materials, Ufa State Aviation Technical University, Ufa, Russian Federation
b Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
c N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (194 kB) Citations (3)
Abstract: N-Allyl-N-methylanilines react with methyl diazoacetate or diazoacetone in the presence of Y, Sc or Sm triflates to give the corresponding methyl N-(2-allylaryl)-N-methylglycinates or 2-allyl-N-methyl-N-(2-oxopropyl)aniline. The formation of these compounds involves the aza-Claisen rearrangement.
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Document Type: Article
Language: English


Citation: A. G. Badamshin, L. V. Spirikhin, R. F. Salikov, V. A. Dokichev, Yu. V. Tomilov, “Lewis acid-catalyzed reactions of N-allylanilines with diazo compounds involving aza-Claisen rearrangement”, Mendeleev Commun., 25:6 (2015), 438–439
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  • https://www.mathnet.ru/eng/mendc/v25/i6/p438
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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