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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Peer reviewed

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 and Adam Daïch

Synthesis (Stuttgart), Vol.47(22), pp.3583-3592

04/11/2015

Analytical chemistry

Catalysis

Chemical Sciences

Medicinal Chemistry

Organic chemistry

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Title: 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
Creators - without role: Ata Martin Lawson - Université Le Havre Normandie
Lahssen El Blidi - Université Le Havre Normandie
Aurélie Namoune - Université Le Havre Normandie
Alexandre Bridoux - Université Le Havre Normandie
Vijaykumar Nimbarte - Université Le Havre Normandie
Ata Lawson - Université Le Havre Normandie
Sébastien Comesse - Université Le Havre Normandie
Adam Daïch - Université Le Havre Normandie
Publication Details: Synthesis (Stuttgart), Vol.47(22), pp.3583-3592
Publisher: Georg Thieme Verlag
Identifiers: 9948832408331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article