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
© 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 c...
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th-cmuir.6653943832-569902018-09-05T03:33:20Z 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 Mookda Pattarawarapan Sirawit Wet-Osot Dolnapa Yamano Wong Phakhodee Chemistry © 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. 2018-09-05T03:33:20Z 2018-09-05T03:33:20Z 2017-03-15 Journal 14372096 09365214 2-s2.0-85003823221 10.1055/s-0036-1588125 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85003823221&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/56990 |
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Chemistry Mookda Pattarawarapan Sirawit Wet-Osot Dolnapa Yamano Wong Phakhodee 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 |
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© 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. |
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Journal |
author |
Mookda Pattarawarapan Sirawit Wet-Osot Dolnapa Yamano Wong Phakhodee |
author_facet |
Mookda Pattarawarapan Sirawit Wet-Osot Dolnapa Yamano Wong Phakhodee |
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Mookda Pattarawarapan |
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 |
title_short |
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 |
title_full |
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 |
title_fullStr |
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 |
title_full_unstemmed |
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 |
title_sort |
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 |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85003823221&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/56990 |
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1681424795316518912 |