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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wong Phakhodee | en_US |
dc.contributor.author | Chuthamat Duangkamol | en_US |
dc.contributor.author | Nittaya Wiriya | en_US |
dc.contributor.author | Mookda Pattarawarapan | en_US |
dc.date.accessioned | 2018-09-05T02:53:46Z | - |
dc.date.available | 2018-09-05T02:53:46Z | - |
dc.date.issued | 2016-01-01 | en_US |
dc.identifier.issn | 18733581 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-84994322327 | en_US |
dc.identifier.other | 10.1016/j.tetlet.2016.10.060 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994322327&origin=inward | en_US |
dc.identifier.uri | http://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.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles | 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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