Abstract
Condensation of dimedone N-methylimine with isopropylidene arylidenemalonates has given 4-aryl-1,7,7-trimethyloctahydroqunoline-2,5-diones, characterized by their IR, UV, and PMR spectra.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature Cited
P. Margaretha,Angew. Chem. 84, 308 (1972).
I. é. Lielbriedis and G. Ya. Dubur, in: The Chemistry of Dicarbonyl Compounds, Reports of the 5th All-Union Conf., Riga (1981), p. 131.
M. F. Strozhev, Ya. A. Miller, and I. é. Lielbriedis, in: The Chemistry of Dicarbonyl Compounds, Reports of the 5th All-Union Conf., Riga (1981), p. 182.
Determination of the Structures of Organic Compounds by Physical and Chemical Methods, Vol. 1 [in Russian], Khimiya, Moscow (1967), p. 532.
O. Ya. Neiland,Izv. Akad. Nauk Latv. SSR, Ser. Khim., No. 5, 577 (1964).
P. Schuster, O. E. Polansky, and F. Wessely,Monatsh. Chem. 95, 53 (1964).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 786–788, June, 1990.
Rights and permissions
About this article
Cite this article
Strozhev, M.F., Lielbriedis, I.É. & Neiland, O.Y. Condensation of dimedone N-methylimine with isopropylidene arylidenemalonates. Chem Heterocycl Compd 26, 655–657 (1990). https://doi.org/10.1007/BF00756417
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00756417