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- W2085871011 abstract "N-substituted 4,5,8(1H)-quinolinetriones react with 1-dimethylamino-1-azadienes giving 1,8-diazaanthracene-4,9,10-triones or 9,10-dihydroxy-1,8-diazaanthracene-4,9,10-triones as the main reaction products. The outcome of the reaction depends on the nature of the N-substituent on the quinone and on the position of substituents on the azadiene. The regioselectivity of the cycloadditions was high, although lower than in the related reactions of 2,5,8(1H)-quinolinetriones previously studied by our group, leading to the isolation of small amounts of 1,5-diazaanthracene-4,9,10-triones. By manipulation of the experimental conditions, the course of the reaction can be diverted to give furo[2,3-f]quinolines through a multi-step, polar [3+2] cycloaddition." @default.
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- W2085871011 date "1997-08-01" @default.
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- W2085871011 title "Hetero Diels-Alder reactions of 4,5,8(1H)-quinolinetriones" @default.
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- W2085871011 doi "https://doi.org/10.1016/s0040-4020(97)00726-6" @default.
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