Expeditious Synthesis of the Topoisomerase I Inhibitors Isoindolo[2,1-b]isoquinolin-7(5H)-one and the Alkaloid Rosettacin Based on Aryl Radical Cyclization of Enamide Generated by Using N-Acyl­iminium Chemistry - Archive ouverte HAL Access content directly
Journal Articles Synthesis: Journal of Synthetic Organic Chemistry Year : 2015

Expeditious Synthesis of the Topoisomerase I Inhibitors Isoindolo[2,1-b]isoquinolin-7(5H)-one and the Alkaloid Rosettacin Based on Aryl Radical Cyclization of Enamide Generated by Using N-Acyl­iminium Chemistry

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Chemical Sciences Chemical Sciences Analytical chemistry Chemical Sciences Catalysis Chemical Sciences Organic chemistry Chemical Sciences Medicinal Chemistry

Ata Martin Lawson  : Connect in order to contact the contributor

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Submitted on : Thursday, October 24, 2019-9:30:13 PM

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hal-02332633 , version 1 (24-10-2019)

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Ata Martin Lawson, Lahssen El Blidi, Aurélie Namoune, Alexandre Bridoux, Vijaykumar Nimbarte, et al.. Expeditious Synthesis of the Topoisomerase I Inhibitors Isoindolo[2,1-b]isoquinolin-7(5H)-one and the Alkaloid Rosettacin Based on Aryl Radical Cyclization of Enamide Generated by Using N-Acyl­iminium Chemistry. Synthesis: Journal of Synthetic Organic Chemistry, 2015, 47 (22), pp.3583-3592. ⟨10.1055/s-0034-1378811⟩. ⟨hal-02332633⟩

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