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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Main Authors: Wet-osot,S., Duangkamol,C., Pattarawarapan,M., Phakhodee,W.
Format: Article
Published: Springer Wien 2015
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http://cmuir.cmu.ac.th/handle/6653943832/38875
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spelling 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
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Chemistry (all)
spellingShingle 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
description © 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.]
format 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
url 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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