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Polyfuryl(aryl)alkanes and their derivatives 9. Polyfuryl(aryl)methanes in the diels-alder reaction
Authors:N. G. Mikhailyuchenko  A. V. Butin  V. E. Zavodnik  V. G. Kul'nevich
Affiliation:(1) Krasnodar Polytechnic Institute, 350072 Krasnodar
Abstract:The reaction of polyfuryl(aryl)methanes with N-(3,5-dichlorophenyl)maleimide has been studied. It was found that tetrasubstituted methanes do not react. Difurylmethane, gem-difurylethane, gem-difurylethane, and trifurylmethane form mono- and diadducts, and difurylarylmethanes form only monoadducts. The molecular and crystal structure of the diadduct of gem-difurylethane- gem-bis {4-aza-7-methyl-10-oxa-4-(3,5-dichlorophenyl)tricyclo-[5,2,1,0 2,6]deca-8-en-3,5-dion-1-yl}ethane has been studied.For Communication 8, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 751–758, June, 1993.
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