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

Ata Martin Lawson; Lahssen El Blidi; Aurélie Namoune; Alexandre Bridoux; Vijaykumar Nimbarte; Ata Lawson; Sébastien Comesse; Adam Daïch

doi:10.1055/s-0034-1378811

Journal articles

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

Ata Martin Lawson ¹ Lahssen El Blidi ² Aurélie Namoune Alexandre Bridoux ³ Vijaykumar Nimbarte ¹ Ata Lawson Sébastien Comesse ¹ Adam Daïch ¹

1 URCOM - Unité de Recherche en Chimie Organique et Macromoléculaire

2 SEESIB - Synthèse et étude de systèmes à intêret biologique

3 ICPAL - Institut de Chimie Pharmaceutique Albert Lespagnol

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Journal articles

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Chemical Sciences

Chemical Sciences / Analytical chemistry

Chemical Sciences / Catalysis

Chemical Sciences / Organic chemistry

Chemical Sciences / Medicinal Chemistry

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https://hal-normandie-univ.archives-ouvertes.fr/hal-02332633
Contributor : Ata Martin Lawson Connect in order to contact the contributor
Submitted on : Thursday, October 24, 2019 - 9:30:13 PM
Last modification on : Tuesday, September 27, 2022 - 4:04:27 AM

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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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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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