Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54287
Title: Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine
Authors: Sirawit Wet-Osot
Chuthamat Duangkamol
Mookda Pattarawarapan
Wong Phakhodee
Keywords: Chemistry
Issue Date: 28-Jun-2015
Abstract: © 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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937819534&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54287
ISSN: 00269247
Appears in Collections:CMUL: Journal Articles

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