Palladium(II)-catalyzed heterocyclisation of 8-arylethynyl-1,2,3,4-tetrahydroquinolines: a facile route to 2-aryl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Synthesis, Structure-Activity Relationships, and Pharmacological Evaluation of Pyrrolo[3,2,1-ij]quinoline Derivatives: Potent Histamine and Platelet Activating Factor Antagonism and 5-Lipoxygenase Inhibitory Properties. Potential Therapeutic Application in Asthma
2. Pyrrolo[3,2,1- ij ]quinoline derivatives, a 5-HT 2c receptor agonist with selectivity over the 5-HT 2a receptor: potential therapeutic applications for epilepsy and obesity
3. Substituted Indole-5-carboxamides and -acetamides as Potent Nonpeptide GnRH Receptor Antagonists
4. Some 5,6-dihydro-4H-pyrrolo[3,2,1-i,j]quinolines
5. Regiospecific Cyclization of 3-Carbomethoxyindole-1-propanoic Acid onto 7-Position of the Indole Nucleus
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1. Ultrasound mediated synthesis of 6-substituted 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinoline derivatives and their pharmacological evaluation;Arabian Journal of Chemistry;2019-12
2. Room temperature catalytic dehydrogenation of cyclic amines with the liberation of H2 using water as a solvent;Green Chemistry;2019
3. The Synthesis of Certain Phomentrioloxin A Analogues and Their Evaluation as Herbicidal Agents;The Journal of Organic Chemistry;2016-12-27
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5. The Rügheimer–Burrows reaction revisited: facile preparation of 4-alkylisoquinolines and 3,5-dialkylpyridines from (partially) saturated amines;Tetrahedron Letters;2015-06
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