PECULIARITIES OF FORMATION OF DECAHYDROACRIDINE-1,8-DIONES ON THE BASIS OF 1,3-DIOXOCYCLOHEXANE COMPOUNDS IN VARIOUS MEDIA

Authors

  • T. Г. Николаева N. G. Chernyshevsky Saratov State University
  • Ю. М. Щекотихин N. G. Chernyshevsky Saratov State University
  • А. C. Пономарев Saratov Higher Military Engineering Chemical Defence School
  • А. П. Кривенько N. G. Chernyshevsky Saratov State University

DOI:

https://doi.org/10.1007/91

Keywords:

1, 8-dioxodecahydroacridines, 3-(N-methylamino)-2-cyclohexenones, methylene(arylidene)-biscyclohexane-1, 3-diones, 2-cyclohexenones, azacylization, amination

Abstract

The conditions for the formation of N-substituted decahydroacridine-1,8-diones from α-R-methylenebiscyclohexane-1,3-diones and 5,5-dimethyl-3-(N-methylamino)-2-cyclohexen-1-one in ethanol, isopropanol, and DMSO have been studied. Methods have been developed for preparation of 1,8-dioxo-10-methyldecahydroacridines which contain furyl and 5-nitrofuryl substituents at the 9 position.

Authors: T. G. Nikolaeva, Yu. M. Shchekotikhin, A. S. Ponomarev, A. P. Kriven'ko.

English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (4), pp 403-409

http://link.springer.com/article/10.1007/BF02269536

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Published

2013-01-15

Issue

No. 4 (2000)

Section

Original Papers