Mass spectral and pyrolytic studies of some 4,4-disubstituted 1,4-dihydro-2H-3,1-benzoxazin-2-ones.
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概要
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Pyrolysis of 4,4-diaryl-1,4-dihydro-2<I>H</I>-3,1-benzoxazin-2-ones at 230–240 °C gives 9-arylacridines and (2-aminophenyl)diarylmethanes. Their formation correlates well with the mass fragmentation of the respective parent compounds.
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