Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54278
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dc.contributor.authorSubin Jaitaen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-04T10:10:42Z-
dc.date.available2018-09-04T10:10:42Z-
dc.date.issued2015-09-01en_US
dc.identifier.issn14372096en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-84939563711en_US
dc.identifier.other10.1055/s-0034-1381117en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84939563711&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/54278-
dc.description.abstract© Georg Thieme Verlag Stuttgart · New York. A convenient and efficient sonochemical method for methyl esterification of carboxylic acids catalyzed by polymer-supported triAphenylphosphine (PS-Ph3P) is reported. In the presence of 1:0.1:2 molar ratio of 2,4,6-trichloro-1,3,5-triazine/PS-Ph3P/Na2CO3, methyl esters of various carboxylic acids bearing reactive hydroxyl groups as well as acid-or base-labile functionalities could be rapidly prepared (within 10-20 min) in good to excellent yields without necessity to pre-activate the acids. Using the polymer-bound phosphine also allows easy isolation of the products which, in most of the cases, were obtained in high purities without column chromatography.en_US
dc.subjectChemistryen_US
dc.titleUltrasound-Assisted Methyl Esterification of Carboxylic Acids ACatalyzed by Polymer-Supported Triphenylphosphineen_US
dc.typeJournalen_US
article.title.sourcetitleSynletten_US
article.volume26en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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