THE USE OF 8-ACYLOXYQUINOLINE METAL COMPLEX IN THE ACYLATION REACTION AND THE KETONE SYNTHESIS. THE METAL ION PROMOTED REACTIONS OF 8-ACYLOXYQUINOLINE I.
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference11 articles.
1. The Participation of Heavy Metal Ions in the Hydrolysis of Amino Acid Esters1
2. Intramolecular bifunctional catalysis of ester hydrolysis by metal ion and carboxylate in the carboxypeptidase model
3. Metal Ion Promoted Hydrolysis of Glycine Amide and of Phenylalanylglycine Amide
4. Metal-ion Sensitive Protecting Groups in Synthesis. The Carbo-(8-quinoloxy) Substituent and its Removal by Accelerated Hydrolysis
5. Kinetics and Mechanism of the Metal Ion Catalyzed Hydrolysis of 8-Acetoxyquinoline
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1. Acylation of Grignard reagents mediated by N-methylpyrrolidone: A remarkable selectivity for the synthesis of ketones;Organic & Biomolecular Chemistry;2011
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3. Reactions of acyl tributylphosphonium chlorides and dialkyl acylphosphonates with Grignard and organolithium reagents;Tetrahedron;1998-10
4. Reactions of in situ formed acyl tributylphosphonium ions with Grignard reagents as an effective route to ketones from acid chlorides;Tetrahedron Letters;1996-07
5. Synthesis of symmetrical diaryl 1,2-diketones from grignard reagents and 1,1′-Oxalylimidazole;Tetrahedron Letters;1993-06
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