Synthesis of 1,2,3-trisubstituted pyrrolo[3,2-c]quinolines via palladium-catalyzed heteroannulation with internal alkynes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Reversible inhibitors of the gastric (H+/K+)-ATPase. 2. 1-Arylpyrrolo[3,2-c]quinolines: effect of the 4-substituent
2. Reversible inhibitors of the gastric (H+/K+)-ATPase. 1. 1-Aryl-4-methylpyrrolo[3,2-c]quinolines as conformationally restrained analogs of 4-(arylamino)quinolines
3. Mechanism of action of amodiaquine. Synthesis of its indoloquinoline analog
4. Martinelline and Martinellic Acid, Novel G-Protein Linked Receptor Antagonists from the Tropical Plant Martinella iquitosensis (Bignoniaceae)
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1. Microwave‐assisted Synthesis of 5,6,7‐Trisubstituted Pyrrolo[2,3‐ d ]Pyrimidines via Palladium‐catalyzed Heteroannulation with Internal Alkynes;Bulletin of the Korean Chemical Society;2019-09-02
2. Synthesis of pyrrolo-heterocycles via Pd-loaded zeolite catalyzed annulation of o - haloaromatic amine with terminal alkynes;Tetrahedron;2017-11
3. Synthesis, ABTS-Radical Scavenging Activity, and Antiproliferative and Molecular Docking Studies of Novel Pyrrolo[1,2-a]quinoline Derivatives;Synthetic Communications;2015-10-02
4. The Larock Reaction in the Synthesis of Heterocyclic Compounds;Advances in Heterocyclic Chemistry;2015
5. FeCl3-Mediated Three-Component Cascade Reaction: An Effective Approach to the Construction of Highly Functionalized Pyrrolo[1,2-c]quinazolinones;Chemistry - A European Journal;2013-12-30
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