Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine
© 2015 Springer-Verlag Wien Abstract: A facile, efficient, and economic method toward N-acylbenzotriazoles was reported using 2,4,6-trichloro-1,3,5-triazine in combination with triethylamine as a carboxylic acid activator. Through reacting 1H-benzotriazole with the generated triacylated triazine int...
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th-cmuir.6653943832-388752015-06-16T07:54:28Z Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine Wet-osot,S. Duangkamol,C. Pattarawarapan,M. Phakhodee,W. Chemistry (all) © 2015 Springer-Verlag Wien Abstract: A facile, efficient, and economic method toward N-acylbenzotriazoles was reported using 2,4,6-trichloro-1,3,5-triazine in combination with triethylamine as a carboxylic acid activator. Through reacting 1H-benzotriazole with the generated triacylated triazine intermediate, a series of N-acylbenzotriazoles could be rapidly prepared in high yields without column chromatography. Graphical abstract: [Figure not available: see fulltext.] 2015-06-16T07:54:28Z 2015-06-16T07:54:28Z 2015-01-27 Article in Press 00269247 2-s2.0-84922342669 10.1007/s00706-014-1408-1 http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84922342669&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38875 Springer Wien |
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Chemistry (all) Wet-osot,S. Duangkamol,C. Pattarawarapan,M. Phakhodee,W. Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine |
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© 2015 Springer-Verlag Wien Abstract: A facile, efficient, and economic method toward N-acylbenzotriazoles was reported using 2,4,6-trichloro-1,3,5-triazine in combination with triethylamine as a carboxylic acid activator. Through reacting 1H-benzotriazole with the generated triacylated triazine intermediate, a series of N-acylbenzotriazoles could be rapidly prepared in high yields without column chromatography. Graphical abstract: [Figure not available: see fulltext.] |
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Article |
author |
Wet-osot,S. Duangkamol,C. Pattarawarapan,M. Phakhodee,W. |
author_facet |
Wet-osot,S. Duangkamol,C. Pattarawarapan,M. Phakhodee,W. |
author_sort |
Wet-osot,S. |
title |
Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine |
title_short |
Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine |
title_full |
Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine |
title_fullStr |
Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine |
title_full_unstemmed |
Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine |
title_sort |
facile synthesis of n-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine |
publisher |
Springer Wien |
publishDate |
2015 |
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http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84922342669&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38875 |
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