Lichtinduzierte synthese von 2,3-dihydropyrrolo[2,3-b] chinolinen und carbostyrilen aus 1-acetyl-trans-3-(2-aminobenzyliden)-pyrrolidonen-(2)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Photoisomerization of Arylidene Heterocycles: Toward the Formation of Fused Heterocyclic Quinolines;The Journal of Organic Chemistry;2022-07-08
2. Facile synthesis of functionalized 1H-pyrrolo[2,3-b]quinolines via Ugi four-component reaction followed by Cu-catalyzed aryl-amide, C–N bond coupling;Tetrahedron Letters;2015-02
3. One-pot synthesis of spiropyrroloquinoline-isoindolinone and their aza-analogs via the Ugi-4CR/metal-free intramolecular bis-annulation process;Organic & Biomolecular Chemistry;2015
4. A new entry to the preparation of pyrrolo[2,3-b]quinolines by an aza Wittig/electrocyclic ring-closure/nitrene insertion process;Tetrahedron;1997-03
5. Synthesis of condensed heteroeyelie systems V: 1|H-Indeno[1,2-b]quinolines from plioloehemieal and Acid-Calalyzed rearrangements of trans-2-(2-Aminobenzylidene)-|-indanones;Journal of Heterocyclic Chemistry;1973-12
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