Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine

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: Sirawit Wet-Osot, Chuthamat Duangkamol, Mookda Pattarawarapan, Wong Phakhodee
Format: Journal
Published: 2018
Subjects:
Agricultural and Biological Sciences
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937819534&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/44308
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-443082018-04-25T07:48:03Z Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine Sirawit Wet-Osot Chuthamat Duangkamol Mookda Pattarawarapan Wong Phakhodee Agricultural and Biological Sciences © 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. 2018-01-24T04:40:37Z 2018-01-24T04:40:37Z 2015-06-28 Journal 00269247 2-s2.0-84937819534 10.1007/s00706-014-1408-1 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937819534&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/44308
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
spellingShingle Agricultural and Biological Sciences
Sirawit Wet-Osot
Chuthamat Duangkamol
Mookda Pattarawarapan
Wong Phakhodee
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.
format Journal
author Sirawit Wet-Osot
Chuthamat Duangkamol
Mookda Pattarawarapan
Wong Phakhodee
author_facet Sirawit Wet-Osot
Chuthamat Duangkamol
Mookda Pattarawarapan
Wong Phakhodee
author_sort Sirawit Wet-Osot
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
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937819534&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/44308
_version_ 1681422535515701248

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