Synthesis of Aza-fused Polycyclic Quinolines Through Copper-catalyzed Cascade Reactions
Overview
Chemistry
Affiliations
A new and efficient method for the synthesis of aza-fused polycyclic quinolines (e.g., benzimidazo[1,2-a]quinolines) is described. This protocol includes an intermolecular condensation followed by a copper-catalyzed intramolecular C-N coupling reaction. The method is applied to a wide range of 2-iodo, 2-bromo, and 2-chloro aryl aldehyde substrates to yield the aza-fused polycyclic quinolines in good yields.
Robinson E, Walden D, Fallan C, Greenhalgh M, Cheong P, Smith A Chem Sci. 2017; 7(12):6919-6927.
PMID: 28567263 PMC: 5450589. DOI: 10.1039/c6sc00940a.
Palladium-Catalyzed Highly Regioselective C-3 Arylation of Imidazo[1,5-]pyridine.
Huang C, Giokaris A, Gevorgyan V Chem Lett. 2013; 40(9).
PMID: 24319312 PMC: 3855034. DOI: 10.1246/cl.2011.1053.
RECENT SYNTHETIC DEVELOPMENTS AND APPLICATIONS OF THE ULLMANN REACTION. A REVIEW.
Lin H, Sun D Org Prep Proced Int. 2013; 45(5).
PMID: 24223434 PMC: 3819134. DOI: 10.1080/00304948.2013.816208.
Ring closing and opening reactions leading to aza-polycyclic aromatic compounds.
Kethe A, Li A, Klumpp D Tetrahedron. 2013; 68(16):3357-3360.
PMID: 24143035 PMC: 3797622. DOI: 10.1016/j.tet.2012.02.047.