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dc.contributor.authorSirawit Wet-Osoten_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-04T10:07:41Z-
dc.date.available2018-09-04T10:07:41Z-
dc.date.issued2015-12-16en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-84947599657en_US
dc.identifier.other10.1016/j.tetlet.2015.10.109en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84947599657&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/54096-
dc.description.abstract© 2015 Elsevier Ltd. All rights reserved. The synthesis of N-acylbenzotriazoles has been demonstrated by the 2,4,6-trichloro-1,3,5-triazine (TCT)-mediated condensation of carboxylic acids with 1H-benzotriazole in aqueous media. In saturated aqueous sodium bicarbonate, TCT was found to be relatively stable and functioned as an efficient acid activator in the acyl transfer process. This operationally simple and economic method allows the scalable synthesis of N-acylbenzotriazoles in good to excellent yields.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleTCT-mediated synthesis of N-acylbenzotriazoles in aqueous mediaen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedron Lettersen_US
article.volume56en_US
article.stream.affiliationsChiang Mai Universityen_US
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