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|Title:||Ph<inf>3</inf>P-I<inf>2</inf>mediated aryl esterification with a mechanistic insight|
|Keywords:||Biochemistry, Genetics and Molecular Biology|
Pharmacology, Toxicology and Pharmaceutics
|Abstract:||© 2016 Elsevier Ltd. All rights reserved. In order to better understand the reaction mechanism and to obtain optimal conditions, the Ph3P-I2/Et3N mediated aryl esterification reaction was thoroughly investigated. Using a specific reagent addition sequence, the reaction proceeds remarkably well especially with acidic substrates.31P NMR studies revealed that the formation of an aryloxyphosphonium salt is crucial in governing the reaction path toward the formation of phenolic esters.|
|Appears in Collections:||CMUL: Journal Articles|
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