1. CMU Intellectual Repository
  2. Academic Support Units
  3. Chiang Mai University Library
  4. CMUL: Journal Articles
Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55208
Full metadata record
DC FieldValueLanguage
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorChuthamat Duangkamolen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-05T02:53:05Z-
dc.date.available2018-09-05T02:53:05Z-
dc.date.issued2016-05-11en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-84979486626en_US
dc.identifier.other10.1016/j.tetlet.2016.03.105en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979486626&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55208-
dc.description.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.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titlePh<inf>3</inf>P-I<inf>2</inf>mediated aryl esterification with a mechanistic insighten_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedron Lettersen_US
article.volume57en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.
Show simple item record


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.