Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight

© 2016 Elsevier Ltd. All rights reserved. In order to better understand the reaction mechanism and to obtain optimal conditions, the Ph 3 P-I 2 /Et 3 N mediated aryl esterification reaction was thoroughly investigated. Using a specific reagent addition sequence, the reaction proceeds remarkably well...

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Main Authors: Phakhodee W., Duangkamol C., Pattarawarapan M.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979486626&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/41886
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-418862017-09-28T04:23:54Z Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight Phakhodee W. Duangkamol C. Pattarawarapan M. © 2016 Elsevier Ltd. All rights reserved. In order to better understand the reaction mechanism and to obtain optimal conditions, the Ph 3 P-I 2 /Et 3 N mediated aryl esterification reaction was thoroughly investigated. Using a specific reagent addition sequence, the reaction proceeds remarkably well especially with acidic substrates. 31 P NMR studies revealed that the formation of an aryloxyphosphonium salt is crucial in governing the reaction path toward the formation of phenolic esters. 2017-09-28T04:23:54Z 2017-09-28T04:23:54Z 2016-05-11 Journal 00404039 2-s2.0-84979486626 10.1016/j.tetlet.2016.03.105 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979486626&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41886
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description © 2016 Elsevier Ltd. All rights reserved. In order to better understand the reaction mechanism and to obtain optimal conditions, the Ph 3 P-I 2 /Et 3 N mediated aryl esterification reaction was thoroughly investigated. Using a specific reagent addition sequence, the reaction proceeds remarkably well especially with acidic substrates. 31 P NMR studies revealed that the formation of an aryloxyphosphonium salt is crucial in governing the reaction path toward the formation of phenolic esters.
format Journal
author Phakhodee W.
Duangkamol C.
Pattarawarapan M.
spellingShingle Phakhodee W.
Duangkamol C.
Pattarawarapan M.
Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight
author_facet Phakhodee W.
Duangkamol C.
Pattarawarapan M.
author_sort Phakhodee W.
title Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight
title_short Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight
title_full Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight
title_fullStr Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight
title_full_unstemmed Ph<inf>3</inf>P-I<inf>2</inf> mediated aryl esterification with a mechanistic insight
title_sort ph<inf>3</inf>p-i<inf>2</inf> mediated aryl esterification with a mechanistic insight
publishDate 2017
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979486626&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/41886
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