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DC Field | Value | Language |
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dc.contributor.author | Mookda Pattarawarapan | en_US |
dc.contributor.author | Sirawit Wet-Osot | en_US |
dc.contributor.author | Dolnapa Yamano | en_US |
dc.contributor.author | Wong Phakhodee | en_US |
dc.date.accessioned | 2018-09-05T03:33:20Z | - |
dc.date.available | 2018-09-05T03:33:20Z | - |
dc.date.issued | 2017-03-15 | en_US |
dc.identifier.issn | 14372096 | en_US |
dc.identifier.issn | 09365214 | en_US |
dc.identifier.other | 2-s2.0-85003823221 | en_US |
dc.identifier.other | 10.1055/s-0036-1588125 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85003823221&origin=inward | en_US |
dc.identifier.uri | http://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.subject | Chemistry | en_US |
dc.title | Mechanochemical 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 Triphenylphosphine | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Synlett | en_US |
article.volume | 28 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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