Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55208
Title: Ph<inf>3</inf>P-I<inf>2</inf>mediated aryl esterification with a mechanistic insight
Authors: Wong Phakhodee
Chuthamat Duangkamol
Mookda Pattarawarapan
Keywords: Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Issue Date: 11-May-2016
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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979486626&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/55208
ISSN: 18733581
00404039
Appears in Collections:CMUL: Journal Articles

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