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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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 6 scientific papers (total in 6 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 (6)

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.

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

Linking options:

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

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

This publication is cited in the following 6 articles:

Feng-Ting Liu, Shuo Wang, Yong-Shun Chen, Jun-Ying Miao, Bao-Xiang Zhao, Zhao-Min Lin, “Facile one-pot synthesis of novel imidates as multifunctional organic fluorescent materials”, Org. Chem. Front., 12:1 (2025), 97
Elghareeb E. Elboray, Taeho Bae, Kotaro Kikushima, Yasuyuki Kita, Toshifumi Dohi, “Transition Metal‐FreeO‐Arylation ofN‐Alkoxybenzamides Enabled by Aryl(trimethoxyphenyl)iodonium Salts”, Adv Synth Catal, 365:16 (2023), 2703
Damiano Tanini, Tommaso Pecchi, Nikolai Ignat'ev, Antonella Capperucci, “Ionic Liquids-Assisted Ring Opening of Three-Membered Heterocycles with Thio- and Seleno-Silanes”, Catalysts, 12:10 (2022), 1259
M. G. Chernysheva, A. E. Averina, O. A. Soboleva, G. A. Badun, “Radionuclide and tensiometry approaches to studying lysozyme behaviors in water–ionic liquid systems”, Mendeleev Commun., 27:3 (2017), 296–298
S. V. Savilov, A. O. Artemova, A. S. Ivanov, Z. Shen, S. M. Aldoshin, V. V. Lunin, “Stability of a high-voltage ionic liquid with a substituted piperidinium cation and a TFSI anion, promising for electrochemical applications”, Mendeleev Commun., 26:3 (2016), 240–242
Margarita A. Epishina, Alexander S. Kulikov, Nikolai V. Ignat'ev, Michael Schulte, Nina N. Makhova, “ChemInform Abstract: Efficient Synthesis of Tertiary Acyclic Amides by the Chapman Rearrangement of Aryl Benzimidates in Ionic Liquids.”, ChemInform, 46:33 (2015)

Citing articles in Google Scholar: Russian citations, English citations
Related articles in Google Scholar: Russian articles, English articles

Mendeleev Communications

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