1984
DOI: 10.1002/chin.198433172
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ChemInform Abstract: DIOXOPYRROLINES. XXVII. SYNTHESES OF 2‐ARYL‐3‐ETHOXYCARBONYL‐ Δ2‐PYRROLINE‐4,5‐DIONES

Abstract: Die aus β‐Ketoestern (I) durch Umsetzung mit Aminen (II) in Essigsäure hergestellten Enaminoester (III) cyclisieren mit Oxalylchlorid (IV) zu Dioxopyrroli‐ nen (V).

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“…In the reaction of substituted 4,5‐dihydro‐1 H ‐pyrroles 292 [283] with arylaminodimethylcyclohexenones 293 in a 1 : 1 molar ratio in boiling anhydrous m ‐xylene, the corresponding spiro‐fused pyrrolo‐tetrahydroacridinones 294 were synthesized in good yields. Presumably, compounds 294 are formed through initial nucleophilic addition of the activated ortho ‐carbon atom in the arylamino group of cyclic enamine 293 to the C(4) carbonyl atom of the pyrrole ring in 292 .…”
Section: Synthesis Of Spirocyclic Quinoxaline Acridine Benzoxazinementioning
confidence: 99%
“…In the reaction of substituted 4,5‐dihydro‐1 H ‐pyrroles 292 [283] with arylaminodimethylcyclohexenones 293 in a 1 : 1 molar ratio in boiling anhydrous m ‐xylene, the corresponding spiro‐fused pyrrolo‐tetrahydroacridinones 294 were synthesized in good yields. Presumably, compounds 294 are formed through initial nucleophilic addition of the activated ortho ‐carbon atom in the arylamino group of cyclic enamine 293 to the C(4) carbonyl atom of the pyrrole ring in 292 .…”
Section: Synthesis Of Spirocyclic Quinoxaline Acridine Benzoxazinementioning
confidence: 99%