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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Piyawat Paengphua | en_US |
dc.contributor.author | Sirirat Chancharunee | en_US |
dc.date.accessioned | 2018-11-29T07:36:19Z | - |
dc.date.available | 2018-11-29T07:36:19Z | - |
dc.date.issued | 2018-10-01 | en_US |
dc.identifier.issn | 00269247 | en_US |
dc.identifier.other | 2-s2.0-85052616175 | en_US |
dc.identifier.other | 10.1007/s00706-018-2238-3 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052616175&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/62627 | - |
dc.description.abstract | © 2018, Springer-Verlag GmbH Austria, part of Springer Nature. Abstract: A simple and efficient procedure for the synthesis of substituted imidazo[1,2-a]pyridines under ultrasound irradiation has been developed. The reactions were carried out using ionic liquids as catalyst. The reaction procedure demonstrated a broad substrate scope for both acetophenones and 2-aminopyridines, and provided convenient access to a wide variety of imidazo[1,2-a]pyridines. The present method offers several advantages compared to traditional heating methods such as higher yields, shorter reaction times, milder reaction conditions, and easier work-up procedure. Graphical abstract: [Figure not available: see fulltext.]. | en_US |
dc.subject | Chemistry | en_US |
dc.title | Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Monatshefte fur Chemie | en_US |
article.volume | 149 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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