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Five-membered 2,3-dioxo heterocycles: XLIX. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with N-substituted 3-amino-5,5-dimethyl-2-cyclohexenones

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Abstract

Methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates react with N-substituted 3-amino-5,5-dimethyl-2-cyclohexenones to give 4′-hydroxy-1′-aryl-3′-aroyl-6,6-dimethyl-1′, 2,3,4,5,5′,6,7-octahydro-1H,2′H-indole-3-spiro-2′-pyrrole-2,4,5′-triones. The structure of the products was proved by the X-ray diffraction data for the 1-cyclohexyl derivative.

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Authors and Affiliations

  1. Perm State University, ul. Bukireva 15, Perm, 614990, Russia

    Yu. N. Bannikova & A. N. Maslivets

  2. Institute of Chemical Physics Problems, Russian Academy of Sciences, Chernogolovka, Moscow oblast, Russia

    Z. G. Aliev

Authors
  1. Yu. N. Bannikova
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  2. A. N. Maslivets
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  3. Z. G. Aliev
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Translated from Zhurnal Organicheskoi Khimii, Vol. 40, No. 12, 2004, pp. 1840–1845.

Original Russian Text Copyright © 2004 by Bannikova, Maslivets, Aliev.

For communication XLVIII, see [1].

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Bannikova, Y.N., Maslivets, A.N. & Aliev, Z.G. Five-membered 2,3-dioxo heterocycles: XLIX. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with N-substituted 3-amino-5,5-dimethyl-2-cyclohexenones. Russ J Org Chem 40, 1791–1797 (2004). https://doi.org/10.1007/s11178-005-0101-6

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  • DOI: https://doi.org/10.1007/s11178-005-0101-6

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