6,6-Dimethyl-4,8-dioxospiro[2.5]octane-1,1,2,2-tetracarbonitrile in the synthesis of heterocyclic compounds of the 2,3-dihydrofuran and 5,6,7,8-tetrahydro-4H-chromene series
Abstract
6,6-Dimethyl-4,8-dioxospiro[2.5]octane-1,1,2,2-tetracarbonitrile (III), synthesized by the interaction of tetracyanoethylene with 2-bromo-5,5-dimethyl-1,3-cyclohexanedione, reacts with alcohols and ketoximes to form 2-alkoxy-2-(3-alkoxycarbonyl-2,2-dimethylpropyl)-5-amino-3-dicyanomethylene-4-cyano-2,3-dihydrofurans and 2-alkylidenaminoxy-2-(3-alkylidenaminoxycarbonyl-2,2-dimethylpropyl)-5-amino-3-dicyanomethylene-4-cyano-2,3-dihydrofurans. Compound III with triarylphosphines forms 2-(triarylphosphoranilidenamino)-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3,4,4-tricarbonitriles.
How to Cite
Kayukova, O. V.; Lukin, P. M.; Kayukov, Y. S.; Nasakin, O. E.; Khrustalev, V. N.; Nesterov, V. N.; Antipin, M. Yu. Chem. Heterocycl. Compd. 1998, 34, 148. [Khim. Geterotsikl. Soedin. 1998, 34, 170.]
For this article in the English edition, see DOI https://doi.org/10.1007/BF02315175