Please use this identifier to cite or link to this item:
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54287Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sirawit Wet-Osot | en_US |
| dc.contributor.author | Chuthamat Duangkamol | en_US |
| dc.contributor.author | Mookda Pattarawarapan | en_US |
| dc.contributor.author | Wong Phakhodee | en_US |
| dc.date.accessioned | 2018-09-04T10:10:54Z | - |
| dc.date.available | 2018-09-04T10:10:54Z | - |
| dc.date.issued | 2015-06-28 | en_US |
| dc.identifier.issn | 00269247 | en_US |
| dc.identifier.other | 2-s2.0-84937819534 | en_US |
| dc.identifier.other | 10.1007/s00706-014-1408-1 | en_US |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937819534&origin=inward | en_US |
| dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/54287 | - |
| dc.description.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. | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine | en_US |
| dc.type | Journal | en_US |
| article.title.sourcetitle | Monatshefte fur Chemie | en_US |
| article.volume | 146 | en_US |
| article.stream.affiliations | Chiang Mai University | en_US |
| Appears in Collections: | CMUL: Journal Articles | |
Files in This Item:
There are no files associated with this item.
Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.