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Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/53328
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dc.contributor.authorBannarak Khumraksaen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-04T09:47:04Z-
dc.date.available2018-09-04T09:47:04Z-
dc.date.issued2014-01-01en_US
dc.identifier.issn20462069en_US
dc.identifier.other2-s2.0-84901257342en_US
dc.identifier.other10.1039/c4ra02969ken_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84901257342&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53328-
dc.description.abstractUltrasound-assisted solventless oxidation/reductive amination of benzyl halides was developed as a facile, efficient, and environmental friendly method toward N-alkylated amines. Aldehydes were formed in situ by oxidation of organic halides with N-methylmorpholine N-oxide (NMO), followed by direct reductive amination with amines using sodium borohydride and montmorillonite K-10 catalyst as the reducing system. This green and simple procedure enables N-alkylated amines to be prepared in good to excellent yields with high selectivity of the monoalkylation. This journal is © the Partner Organisations 2014.en_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleUltrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halidesen_US
dc.typeJournalen_US
article.title.sourcetitleRSC Advancesen_US
article.volume4en_US
article.stream.affiliationsChiang Mai Universityen_US
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