M. I. Pleshchev, M. A. Epishina, V. V. Kachala, V. V. Kuznetsov, A. S. Goloveshkin, I. S. Bushmarinov, N. N. Makhova, “Ionic liquid-promoted stereoselective [3 + 2] cycloaddition of 1-hetaryl-2-nitroethenes to azomethine imines generated in situ”, Mendeleev Commun., 23:4 (2013), 206

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Mendeleev Communications, 2013, Volume 23, Issue 4, Pages 206–208
DOI: https://doi.org/10.1016/j.mencom.2013.07.009 (Mi mendc2663)

This article is cited in 10 scientific papers (total in 10 papers)

Communications

Ionic liquid-promoted stereoselective [3 + 2] cycloaddition of 1-hetaryl-2-nitroethenes to azomethine imines generated in situ

M. I. Pleshchev^a, M. A. Epishina^a, V. V. Kachala^a, V. V. Kuznetsov^a, A. S. Goloveshkin^b, I. S. Bushmarinov^b, N. N. Makhova^a

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation

Full-text PDF (376 kB) Citations (10)

DOI: https://doi.org/10.1016/j.mencom.2013.07.009

Abstract: Ionic liquids facilitate regio- and stereoselective [3 + 2] cycloaddition of 1-hetaryl-2-nitroethenes to azomethine imines generated catalytically from 6-Ar-1,5-diazabicyclo[3.1.0]hexanes in the presence of BF₃ Et₂O. The similar reaction is possible in MeCN only for azomethine imine with Ar = 2,4-(MeO)₂C₆H₃ to give a mixture of two diastereomers.

Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(210.3 Kb)

Citation: M. I. Pleshchev, M. A. Epishina, V. V. Kachala, V. V. Kuznetsov, A. S. Goloveshkin, I. S. Bushmarinov, N. N. Makhova, “Ionic liquid-promoted stereoselective [3 + 2] cycloaddition of 1-hetaryl-2-nitroethenes to azomethine imines generated in situ”, Mendeleev Commun., 23:4 (2013), 206–208

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This publication is cited in the following 10 articles:

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

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