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dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorChuthamat Duangkamolen_US
dc.contributor.authorNittaya Wiriyaen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-05T02:53:46Z-
dc.date.available2018-09-05T02:53:46Z-
dc.date.issued2016-01-01en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-84994322327en_US
dc.identifier.other10.1016/j.tetlet.2016.10.060en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994322327&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55263-
dc.description.abstract© 2016 Elsevier Ltd A sonochemical method for the synthesis of 2-aminobenzimidazoles and 2-aminobenzoxazoles, as well as chiral aminooxazolines and a chiral substituted quinazolin-5-one is reported. Using the Ph3P–I2system in the presence of triethylamine as a desulfurization agent, monothioureas prepared in situ from the reaction of bis-nucleophiles with isothiocyanates underwent rapid cyclization to afford a variety of N-heterocyclic compounds in good to excellent yields under mild conditions.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleUltrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocyclesen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedron Lettersen_US
article.volume57en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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