Synthesis of bis-benzoquinoline derivatives catalyzed by iodine via ring-opening of furan

Add time:08/25/2019    Source:sciencedirect.com

A three-component reaction of aromatic aldehyde, naphthalene-2-amine, and tetrahydro-2,5-dimethoxyfuran in methanol catalyzed by iodine, is described in this paper. With the ring-opening of furan, a series of 3-aryl-2-(3-arylbenzo[f]quinolin-2-yl)benzo[f]quinoline derivatives were obtained in moderate yields.

We also recommend Trading Suppliers and Manufacturers of (TETRAHYDRO-FURAN-3-YL)-ACETIC ACID (cas 138498-97-2). Pls Click Website Link as below: cas 138498-97-2 suppliers

Prev:Short communicationSolid acid catalyzed aldol dimerization of levulinic acid for the preparation of C10 renewable fuel and chemical feedstocks
Next:Research paperQuantum dynamics studies of the Na(3S) + HF and Na(3S/3P) + DF reactions: The effects of the initial rotational excitation and the isotopic substitution)