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Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/70401
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dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorDolnapa Yamanoen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2020-10-14T08:29:12Z-
dc.date.available2020-10-14T08:29:12Z-
dc.date.issued2020-04-22en_US
dc.identifier.issn14372096en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-85082668479en_US
dc.identifier.other10.1055/s-0039-1691583en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082668479&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70401-
dc.description.abstract© 2020 Georg Thieme Verlag. All rights reserved. A convenient ultrasound-assisted one-pot synthesis of N -acylcyanamides starting from readily available carboxylic acids and sodium cyanamide has been developed. Upon activation in the presence of trichloroisocyanuric acid (TCCA) and triphenylphosphine, a range of carboxylic acids was converted into N -acylcyanamides in good to excellent yields within 10 minutes at room temperature without base. Remarkably, N -acyl-substituted imidazolones were readily accessible through guanylation-cyclization of the in situ generated N -acylcyanamides.en_US
dc.subjectChemistryen_US
dc.titleUltrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphineen_US
dc.typeJournalen_US
article.title.sourcetitleSynletten_US
article.volume31en_US
article.stream.affiliationsChiang Mai Universityen_US
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