A convenient synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones under solvent-assisted grinding

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DC Field	Value	Language
dc.contributor.author	Mookda Pattarawarapan	en_US
dc.contributor.author	Subin Jaita	en_US
dc.contributor.author	Wong Phakhodee	en_US
dc.date.accessioned	2018-09-05T02:53:45Z	-
dc.date.available	2018-09-05T02:53:45Z	-
dc.date.issued	2016-01-01	en_US
dc.identifier.issn	18733581	en_US
dc.identifier.issn	00404039	en_US
dc.identifier.other	2-s2.0-84975853310	en_US
dc.identifier.other	10.1016/j.tetlet.2016.06.029	en_US
dc.identifier.uri	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84975853310&origin=inward	en_US
dc.identifier.uri	http://cmuir.cmu.ac.th/jspui/handle/6653943832/55262	-
dc.description.abstract	© 2016 Elsevier Ltd A facile and effective approach for the synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones has been developed. Under solvent-assisted grinding in the presence of 2,4,6-trichloro-1,3,5-triazine, catalytic triphenylphosphine, and sodium carbonate, dehydration–condensation of hippuric acid with aromatic aldehydes proceeded rapidly within minutes at room temperature to afford the products in good to excellent yields.	en_US
dc.subject	Biochemistry, Genetics and Molecular Biology	en_US
dc.subject	Chemistry	en_US
dc.subject	Pharmacology, Toxicology and Pharmaceutics	en_US
dc.title	A convenient synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones under solvent-assisted grinding	en_US
dc.type	Journal	en_US
article.title.sourcetitle	Tetrahedron Letters	en_US
article.volume	57	en_US
article.stream.affiliations	Chiang Mai University	en_US
Appears in Collections:	CMUL: Journal Articles

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