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dc.contributor.authorSubin Jaitaen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorNeeranuch Chairungsien_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-11-29T07:32:29Z-
dc.date.available2018-11-29T07:32:29Z-
dc.date.issued2018-09-26en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-85052623821en_US
dc.identifier.other10.1016/j.tetlet.2018.08.035en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052623821&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62562-
dc.description.abstract© 2018 A facile and effective approach toward the synthesis of primary amides from carboxylic acids has been developed. In the presence of 2,4,6-trichloro-1,3,5-triazine, a combination of ammonium thiocyanate and potassium carbonate led to the rapid conversion of carboxylic acids into the corresponding amides within five minutes grinding at room temperature. The use of ammonium thiocyanate as the amine source is unprecedented and exclusive formation of primary amides is observed only under the liquid-assisted grinding conditions.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleMechanochemical synthesis of primary amides from carboxylic acids using TCT/NH<inf>4</inf>SCNen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedron Lettersen_US
article.volume59en_US
article.stream.affiliationsRajamangala University of Technology Lannaen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsChiang Mai Rajabhat Universityen_US
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