Five-membered 2,3-dioxo heterocycles: C. Reaction of methyl 1-aryl-3-cinnamoyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carbocylates with acyclic enamines

Five-membered 2,3-dioxo heterocycles: C. Reaction of methyl 1-aryl-3-cinnamoyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carbocylates with acyclic enamines

Methyl 1-aryl-3-cinnamoyl-4,5-dioxo-4,5-dihydro-1 H -pyrrole-2-carbocylates react with N-substituted ethyl 3-amino-3-phenylprop-2-enoates, ethyl 3-aminobut-2-enoates, 3-amino-1,3-diphenylprop-2-en-1-ones, and dimethyl 2-arylaminofumarates to give 9-ethoxycarbonyl-, 9-benzoyl-, and 8,9-bis(methoxycar...

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Veröffentlicht in:Russian journal of organic chemistry 2014-03, Vol.50 (3), p.406-411
Hauptverfasser: Silaichev, P. S., Filimonov, V. O., Maslivets, A. N.
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container_end_page 411
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container_title Russian journal of organic chemistry
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creator Silaichev, P. S.
Filimonov, V. O.
Maslivets, A. N.
description Methyl 1-aryl-3-cinnamoyl-4,5-dioxo-4,5-dihydro-1 H -pyrrole-2-carbocylates react with N-substituted ethyl 3-amino-3-phenylprop-2-enoates, ethyl 3-aminobut-2-enoates, 3-amino-1,3-diphenylprop-2-en-1-ones, and dimethyl 2-arylaminofumarates to give 9-ethoxycarbonyl-, 9-benzoyl-, and 8,9-bis(methoxycarbonyl)-4-cinnamoyl-1,7-diazaspiro[4.4]nona-3,8-dienes.
doi_str_mv 10.1134/S107042801403018X
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Organic Chemistry
title Five-membered 2,3-dioxo heterocycles: C. Reaction of methyl 1-aryl-3-cinnamoyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carbocylates with acyclic enamines
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