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- W2091925640 abstract "4.5-Benzo-oxepin-2.7-dicarbonsauredimethylester (VI) nimmt nur 1 Mol Brom auf. Die freie Dicarbonsaure decarboxyliert bei 300° unter Ringkontraktion zu 2-Hydroxy-naphthoesaure-(3). Einige Versuche mit 1-Phenyl-4.5-benzo-azepin-2.7-dicarbonsaure (XII) werden beschrieben. Die Paal-Knorrsche Pyrrol-synthese sollte, ausgehend vom Vinylogen der γ-Dicarbonylverbindung, Azepine liefern; Versuche mit o-Phenylen-diacetaldehyd, o-Phenylen-diacetonitril und mit cis-Dihydromucon-dialdehyd waren nicht erfolgreich." @default.
- W2091925640 created "2016-06-24" @default.
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- W2091925640 date "1960-05-17" @default.
- W2091925640 modified "2023-10-12" @default.
- W2091925640 title "Syntheseversuche in der Oxepin- und Azepin-Reihe" @default.
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- W2091925640 doi "https://doi.org/10.1002/jlac.19606300116" @default.
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