EventsThe 19th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 19th International Electronic Conference on Synthetic Organic Chemistry
Published date
05 Nov, 2015
Citation
Eric DENIAU, Stéphane LEBRUN, Chiral phase-transfer catalyzed intramolecular aza-Michael reactions for the asymmetric synthesis of isoindolinones, in Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2015, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-19-a057
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Chiral phase-transfer catalyzed intramolecular aza-Michael reactions for the asymmetric synthesis of isoindolinones

1. Unité de Catalyse et de Chimie du Solide (UCCS) UMR CNRS 8181 - Axe CCM - Equipe CASECO
Abstract

Asymmetric intramolecular aza-Michael reactions catalyzed by cinchoninium phase-transfer organocatalysts are used for the synthesis of optically active isoindolinones. Selected oligomeric cinchoninium salts proved to be efficient and selective catalysts for the intramolecular addition of alkenylated benzamide substrates. The resulting compounds are useful intermediates for the synthesis and development of benzodiazepine-receptor agonists.

Keywords
Organocatalysis
phase-transfer catalysis
aza-Michael
heterocycle
isoindolinone
Manuscript
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