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dc.contributor.authorMookda Pattarawarapanen_US
dc.contributor.authorSubin Jaitaen_US
dc.contributor.authorSirilak Wangngaeen_US
dc.contributor.authorWong Phakhodeeen_US
dc.date.accessioned2018-09-05T02:53:22Z-
dc.date.available2018-09-05T02:53:22Z-
dc.date.issued2016-03-23en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-84975822864en_US
dc.identifier.other10.1016/j.tetlet.2016.02.050en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84975822864&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55229-
dc.description.abstract© 2016 Elsevier Ltd Ultrasound-assisted synthesis of guanidine derivatives was developed using 2,4,6-trichloro-1,3,5-triazine as an inexpensive dehydrosulfurization reagent. Both 1,3-alkylaryl- and 1,3-diaryl-thioureas were rapidly converted into carbodiimides before subsequent reaction with aromatic or aliphatic amines. The method allows rapid access to highly substituted guanidines in good to excellent yields under mild conditions and with minimal use of solvent.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleUltrasound-assisted synthesis of substituted guanidines from thioureasen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedron Lettersen_US
article.volume57en_US
article.stream.affiliationsChiang Mai Universityen_US
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