Recyclization of 5-Aryl-1H-pyrrole-2,3-diones with Amidoximes. Synthesis of Enamines Containing a 1,2,4-Oxadiazole Fragment
5-Aryl-1 H -pyrrole-2,3-diones reacted with amidoximes to give enamines containing a 1,2,4-oxadiazole fragment that are potential precursors to novel 1 H -pyrrole-2,3-diones. The described reaction is the first example of recyclization of 4-unsubstitued 5-aryl-1 H -pyrrole-2,3-diones by the action...
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Veröffentlicht in: | Russian journal of organic chemistry 2024-03, Vol.60 (3), p.387-390 |
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container_title | Russian journal of organic chemistry |
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creator | Antonov, D. I. Dmitriev, M. V. Kuchumov, I. A. Maslivets, A. N. |
description | 5-Aryl-1
H
-pyrrole-2,3-diones reacted with amidoximes to give enamines containing a 1,2,4-oxadiazole fragment that are potential precursors to novel 1
H
-pyrrole-2,3-diones. The described reaction is the first example of recyclization of 4-unsubstitued 5-aryl-1
H
-pyrrole-2,3-diones by the action of 1,4-binucleophiles. |
doi_str_mv | 10.1134/S1070428024030023 |
format | Article |
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H
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H
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H
-pyrrole-2,3-diones reacted with amidoximes to give enamines containing a 1,2,4-oxadiazole fragment that are potential precursors to novel 1
H
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H
-pyrrole-2,3-diones reacted with amidoximes to give enamines containing a 1,2,4-oxadiazole fragment that are potential precursors to novel 1
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source | Springer Online Journals |
subjects | Aromatic compounds Chemistry Chemistry and Materials Science Organic Chemistry Oxadiazoles |
title | Recyclization of 5-Aryl-1H-pyrrole-2,3-diones with Amidoximes. Synthesis of Enamines Containing a 1,2,4-Oxadiazole Fragment |
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