Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/56990
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dc.contributor.authorMookda Pattarawarapanen_US
dc.contributor.authorSirawit Wet-Osoten_US
dc.contributor.authorDolnapa Yamanoen_US
dc.contributor.authorWong Phakhodeeen_US
dc.date.accessioned2018-09-05T03:33:20Z-
dc.date.available2018-09-05T03:33:20Z-
dc.date.issued2017-03-15en_US
dc.identifier.issn14372096en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-85003823221en_US
dc.identifier.other10.1055/s-0036-1588125en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85003823221&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/56990-
dc.description.abstract© Georg Thieme VerlagStuttgart · New York. A mild and convenient approach for the synthesis of 2-substituted 4H-3,1-benzoxazin-4-ones, 2-aminobenzoxazin-4-ones, and 2-amino-4H-3,1-benzothiazin-4-ones under solvent-assisted grinding is reported. In the presence of 2,4,6-trichloro-1,3,5-triazine and catalytic triphenylphosphine, cyclodehydration of N-substituted anthranilic acid derivatives proceeded rapidly within minutes at room temperature. The products were also obtained in good to excellent yields by using minimal amounts of solvent and inexpensive reagents.en_US
dc.subjectChemistryen_US
dc.titleMechanochemical Synthesis of Substituted 4H-3,1-Benzoxazin-4-ones, 2-Aminobenzoxazin-4-ones, and 2-Amino-4H-3,1-benzothiazin-4-ones Mediated by 2,4,6-Trichloro-1,3,5-triazine and Triphenylphosphineen_US
dc.typeJournalen_US
article.title.sourcetitleSynletten_US
article.volume28en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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