Electroreductive intermolecular coupling of phthalimides with aldehydes: application to the synthesis of alkylideneisoindolin-1-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. Novel and stereoselective methods for the preparation of aromatic lactams via reductive coupling reactions mediated by SmI2
2. A novel synthetic approach to isoindolobenzazepine alkaloid, chilenine, employing SmI2-mediated pinacolic coupling reaction
3. Ketone-Imide versus Ketone-Oxime Reductive Cross-Coupling Promoted by Samarium Diiodide: New Mechanistic Insight Gained from a Failed Aminocyclopentitol Synthesis
4. Phthalimides as Exceptionally Efficient Single Electron Transfer Acceptors in Reductive Coupling Reactions Promoted by Samarium Diiodide
5. Electroreductive intramolecular coupling of N-(oxoalkyl)phthalimides: complementary method to samarium(II) iodide reduction
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1. Synthesis and Wittig olefination of (2-methyl-3-oxoisoindolin-1-yl)triphenylphosphonium tetrafluoroborate: facile access to 3-alkylidene-2-methylisoindolin-1-ones;Phosphorus, Sulfur, and Silicon and the Related Elements;2023-09-25
2. Ultrasound-assisted-one-pot synthesis and antiplasmodium evaluation of 3-substituted-isoindolin-1-ones;RSC Advances;2023
3. Photoredox Hydroxy-arylation of the Terminal Double Bond of N-Substituted 3-Methyleneisoindolin-1-ones in Visible Light;The Journal of Organic Chemistry;2022-08-30
4. Electrochemical formal homocoupling of sec-alcohols;Beilstein Journal of Organic Chemistry;2022-08-22
5. Samarium(ii)-electrocatalyzed chemoselective reductive alkoxylation of phthalimides;Organic Chemistry Frontiers;2022
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