A new entry to the preparation of pyrrolo[2,3-b]quinolines by an aza Wittig/electrocyclic ring-closure/nitrene insertion process
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Regiospecific preparation of γ-carbolines andpyrimido[3, 4-a]indole derivatives by intramolecular ring-closure of heterocumulene-substituted indoles
2. Pyrroloquinolines I. 1H-Pyrrolo[2,3-b]quinolines
3. Lichtinduzierte synthese von 2,3-dihydropyrrolo[2,3-b] chinolinen und carbostyrilen aus 1-acetyl-trans-3-(2-aminobenzyliden)-pyrrolidonen-(2)
4. Pyrroloquinolines - Part 1. Synthesis of 1-Aryl-2-chloro-1H-pyrrolo[2,3-b]quinolines
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1. Cyclocondensation of 5-chloro-4-formylpyrrole-3-carboxylates with arylamines. Synthesis and fluorescent properties of pyrrolo[2,3-b]quinoline-3-carboxylates and their benzo[f] analogs;Chemistry of Heterocyclic Compounds;2021-10
2. Visible-light-driven photocyclization reaction: photocatalyst-free mediated intramolecular N–N coupling for the synthesis of 2H-indazole-3-carboxamides from aryl azides;Organic Chemistry Frontiers;2021
3. Gold(III)-Catalyzed Site-Selective and Divergent Synthesis of 2-Aminopyrroles and Quinoline-Based Polyazaheterocycles;Angewandte Chemie International Edition;2018-11-12
4. Gold(III)-Catalyzed Site-Selective and Divergent Synthesis of 2-Aminopyrroles and Quinoline-Based Polyazaheterocycles;Angewandte Chemie;2018-11-11
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