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Iron-mediated Synthesis of the AntiostatinsKnott, Kerstin 20 March 2009 (has links) (PDF)
Within this thesis the first total syntheses of eight biologically active natural products from the family of carbazole alkaloids, antiostatins A1 to A4 and B2 to B5, were established. Spectroscopic data of the synthesised natural products are in good agreement with the isolated antiostatins from Streptomyces cyaneus 2007-SV1, which confirms the molecular structures assigned to the natural products. The total synthesis of the antiostatins A1 to A4 and B2 to B5 were achieved employing the iron-mediated synthesis to form the carbazole nucleus from a cyclohexadienylium iron salt and appropriate arylamines. This transition metal-mediated approach could be applied to all antiostatins in excellent yields. The antiostatins A1-4 and B2-5 represent the first carbazole alkaloids with an acetamide or substituted biuret chain. Introduction of the sophisticated substituents proceeded selectively on C-4 in high yields. Antiostatins A1 to A4 and B2 to B5 could be synthesised over eight steps from a tricarbonyliron-coordinated cyclohexadienylium salt. The overall yields are in the range of 31 – 63%.
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Iron-mediated Synthesis of the AntiostatinsKnott, Kerstin 16 February 2009 (has links)
Within this thesis the first total syntheses of eight biologically active natural products from the family of carbazole alkaloids, antiostatins A1 to A4 and B2 to B5, were established. Spectroscopic data of the synthesised natural products are in good agreement with the isolated antiostatins from Streptomyces cyaneus 2007-SV1, which confirms the molecular structures assigned to the natural products. The total synthesis of the antiostatins A1 to A4 and B2 to B5 were achieved employing the iron-mediated synthesis to form the carbazole nucleus from a cyclohexadienylium iron salt and appropriate arylamines. This transition metal-mediated approach could be applied to all antiostatins in excellent yields. The antiostatins A1-4 and B2-5 represent the first carbazole alkaloids with an acetamide or substituted biuret chain. Introduction of the sophisticated substituents proceeded selectively on C-4 in high yields. Antiostatins A1 to A4 and B2 to B5 could be synthesised over eight steps from a tricarbonyliron-coordinated cyclohexadienylium salt. The overall yields are in the range of 31 – 63%.
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Novel approach to biscarbazole alkaloids via Ullmann coupling – synthesis of murrastifoline-A and bismurrayafoline-ABörger, Carsten, Kataeva, Olga, Knölker, Hans-Joachim January 2012 (has links)
Unprecedented Ullmann couplings of murrayafoline-A with either 6-bromo- or 4-bromocarbazole derivatives provide highly efficient synthetic routes to the biscarbazole alkaloids murrastifoline-A (6 steps, 66% overall yield) and bismurrayafoline-A (6 steps, 28% overall yield). / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
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First total synthesis of the biscarbazole alkaloid oxydimurrayafolineBörger, Carsten, Krahl, Micha P., Gruner, Margit, Kataeva, Olga, Knölker, Hans-Joachim January 2012 (has links)
We report the first total synthesis of oxydimurrayafoline via nucleophilic substitution at the benzylic position at C-3 of the carbazole framework. / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
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