Abstract
Three-component condensation of 6,6-heptamethylenetetrahydropyran-2,4-dione with 2-amino-naphthalene or 6-aminoquinoline and aromatic aldehydes in an aliphatic alcohol afforded 12-aryl-9,9-hepta-methylene-8,9,10,12-tetrahydro-7H-benzo[f]pyrano[3,4-b]quinolin-11-ones and 12-aryl-9,9-heptamethylene-8,9,10,12-tetrahydro-7H-pyrano[4,3-b][4,7]phenanthrolin-11-ones, new N,O-heterocycles which include azaor diazaphenanthrene system fused to α-pyrone ring and aromatic and spiro substituents.
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Kozlov, N.G., Pashkovskii, F.S., Gusak, K.N. et al. 6,6-Heptamethylenetetrahydropyran-2,4-dione in the Synthesis of Benzo[f]pyrano[3,4-b]quinolines and Pyrano[4,3-b][4,7]phenanthrolines. Russian Journal of Organic Chemistry 40, 555–559 (2004). https://doi.org/10.1023/B:RUJO.0000036079.00169.3b
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DOI: https://doi.org/10.1023/B:RUJO.0000036079.00169.3b