Abstract
In the present investigation, the incorporation of the oxepine ring into a polycyclic-fused quinoline system leading to a series of structurally novel hybrids benzo[h] areno[6,7]oxepino[3,4-b]quinolin-8(14H)-ones has been achieved through a simple, and economical two-step procedure that involves the one-pot synthesis of 2-(aryloxymethyl) benzo[h]quinoline-3-carboxylic acids followed by intramolecular Friedel-Crafts acylation reaction using Eaton's reagent.
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Gao, W., Nie, C., Xu, L., Zhao, B., & Li, Y. (2014). Synthesis of novel oxepine-containing polycyclic-fused quinoline systems. Heterocyclic Communications, 20(3), 161–166. https://doi.org/10.1515/hc-2013-0227
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