M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids”, Mendeleev Commun., 25:2 (2015), 126

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Mendeleev Communications, 2015, Volume 25, Issue 2, Pages 126–128
DOI: https://doi.org/10.1016/j.mencom.2015.03.016 (Mi mendc2322)

This article is cited in 7 scientific papers (total in 7 papers)

Communications

Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids

M. A. Epishina^a, A. S. Kulikov^a, N. V. Ignat'ev^b, M. Schulte^b, N. N. Makhova^a

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b Ionic Liquid Research Laboratory, Merck KGaA, Darmstadt, Germany

Full-text PDF (249 kB) Citations (7)

DOI: https://doi.org/10.1016/j.mencom.2015.03.016

Graphic abstract: Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids

Abstract: The Chapman rearrangement of aryl N-arylbenzimidates to tertiary acyclic amides is accelerated in ionic liquids and proceeds at lower temperatures as 120–190°C.

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Document Type: Article

Language: English

Citation: M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids”, Mendeleev Commun., 25:2 (2015), 126–128

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https://www.mathnet.ru/eng/mendc2322

https://www.mathnet.ru/eng/mendc/v25/i2/p126

This publication is cited in the following 7 articles:

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