Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/74681
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dc.contributor.authorDolnapa Yamanoen_US
dc.contributor.authorNittaya Wiriyaen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorSirawit Wet-Osoten_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2022-10-16T06:46:35Z-
dc.date.available2022-10-16T06:46:35Z-
dc.date.issued2022-09-01en_US
dc.identifier.issn14372096en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-85134747585en_US
dc.identifier.other10.1055/s-0040-1719867en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85134747585&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/74681-
dc.description.abstractMechanochemical synthesis of 2,5-disubstituted 1,3,4-oxadiazoles was developed as an environmentally benign alternative to conventional solvent-based methods. In the presence of triphenylphosphine and trichloroisocyanuric acid, N-acylbenzotriazoles condense with acylhydrazides leading to oxadiazoles derivatives in good to excellent yields within minutes. The approach circumvents the need for strictly anhydrous conditions, external heating, long reaction times, as well as tedious multistep procedures. A range of substrates with reactive functionalities was also well tolerated.en_US
dc.subjectChemistryen_US
dc.titleMechanochemical Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazoles Mediated by PPh <inf>3</inf>-TCCAen_US
dc.typeJournalen_US
article.title.sourcetitleSynletten_US
article.volume33en_US
article.stream.affiliationsThailand Ministry of Public Healthen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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