Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55451
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dc.contributor.authorSirawit Wet-Osoten_US
dc.contributor.authorChuthamat Duangkamolen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-05T02:56:14Z-
dc.date.available2018-09-05T02:56:14Z-
dc.date.issued2016-06-13en_US
dc.identifier.issn21568952en_US
dc.identifier.other2-s2.0-84974539419en_US
dc.identifier.other10.1021/acscombsci.6b00055en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84974539419&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55451-
dc.description.abstract© 2016 American Chemical Society. An ultrasound-assisted one-pot acylation/cyclization reaction between N-acylbenzotriazoles and 2-hydroxybenzaldehydes has been developed for the synthesis of substituted 3-arylcoumarins. Using ultrasound not only allows rapid and clean conversion but also simplifies experimental setup and parallel workup leading to rapid generation of 3-arylcoumarin libraries under mild, solvent-free, and chromatography-free conditions.en_US
dc.subjectChemistryen_US
dc.titleUltrasound-Assisted Solvent-Free Parallel Synthesis of 3-Arylcoumarins Using N-Acylbenzotriazolesen_US
dc.typeJournalen_US
article.title.sourcetitleACS Combinatorial Scienceen_US
article.volume18en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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