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The electron ionization-inducted fragmentation patterns of cis-3a,4,9,9a-tetrahydro-4-methyl-2-phenyl-1H-pyrrolo[3,4-b]quinoline-1,3(2H)-dione derivatives have been studied. It was found that fragmentation starts at N-phenylsuccinimide ring and its pattern depends on the type and position of the substituents at carbon atoms 5-8. Peaks, which can be assigned to the products of the retro Diels-Alder opening of the nitrogen atom containing tetrahydroquinoline ring, were observed.
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Tom
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554--563
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Bibliogr. 9 poz., tab., wykr.
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- Institute of Organic Chemistry Polish Academy of Sciences ul. Kasprzaka 44/52 01-224 Warszawa Poland, witold@ichf.edu.pl
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bwmeta1.element.baztech-article-BAR2-0001-0075