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- W2022817655 abstract "Aus den leicht zuganglichen Indolderivaten 4, 7 und 15 lassen sich durch Grignard-Reaktionen, nukleophile Substitutionen an den entspr. Dithianen und Wittig-Reaktionen variable Seitenketten an C-2 des Indols einfuhren. Durch intramolekulare Michael-Addition entstehen die Pyrrolidino- bzw. Pyrrolino[3,4-c]carbazole 32 und 33.Synthesis of Carbazole Derivatives, II: C-2-substituted Indoles as Intermediates of Pyrrolino[3,4-c]carbazolesStarting from the indole derivatives 4, 7 and 15Grignard reaction, nucleophilic substitution at the pertinent dithian, and Wittig reaction afford preparatively useful side chains. By intramolecular Michael reaction the pertinent compounds lead to the pyrrolidino- and pyrrolino[3,4-c]carbazoles 32 and 33, respectively." @default.
- W2022817655 created "2016-06-24" @default.
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- W2022817655 date "1995-01-01" @default.
- W2022817655 modified "2023-09-26" @default.
- W2022817655 title "Synthese von Carbazolderivaten, 2. Mitt.: 2-Substituierte Indole als Zwischenprodukte von Pyrrolino[3,4-c]carbazolen" @default.
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- W2022817655 doi "https://doi.org/10.1002/ardp.19953280109" @default.
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