Yu. S. Syroeshkina, V. V. Kachala, I. V. Ovchinnikov, V. V. Kuznetsov, Yu. V. Nelyubina, K. A. Lyssenko, N. N. Makhova, “Ionic-liquids-assisted reaction of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with β-nitrostyrenes”, Mendeleev Commun., 2009, Volume 19, Issue 5,Pages <nobr>276

This article is cited in 24 papers

Ionic-liquids-assisted reaction of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with β-nitrostyrenes

Yu. S. Syroeshkina^a, V. V. Kachala^a, I. V. Ovchinnikov^a, V. V. Kuznetsov^a, Yu. V. Nelyubina^b, K. A. Lyssenko^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

Abstract: 5,6-Diaryl-2,3-dihydro-1H-pyrazolo[1,2-a]pyrazolium tetrafluoroborates (hexafluorophosphate) were unexpectedly synthesized along with expected 1,3-diaryl-2-nitrotetrahydro-1H,5H-pyrazolo[1,2-a]pyrazoles, under the action of 1-nitro-2-(3-nitrophenyl)-ethylene on 6-aryl-1,5-diazabicyclo[3.1.0]hexanes in ionic liquids with the Et₂O·BF₃ catalyst, whereas the same reaction with unsubstituted β-nitrostyrene produced only 1,3-diaryl-2-nitrotetrahydro-1H,5H-pyrazolo[1,2-a]pyrazole derivatives.

Language: English

DOI: 10.1016/j.mencom.2009.09.016

	*Supplementary materials:*
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