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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Wong Phakhodee | en_US |
| dc.contributor.author | Sirilak Wangngae | en_US |
| dc.contributor.author | Mookda Pattarawarapan | en_US |
| dc.date.accessioned | 2018-09-05T02:55:07Z | - |
| dc.date.available | 2018-09-05T02:55:07Z | - |
| dc.date.issued | 2016-01-01 | en_US |
| dc.identifier.issn | 20462069 | en_US |
| dc.identifier.other | 2-s2.0-84976633635 | en_US |
| dc.identifier.other | 10.1039/c6ra12801g | en_US |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84976633635&origin=inward | en_US |
| dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/55389 | - |
| dc.description.abstract | © 2016 The Royal Society of Chemistry. A direct amidation of carboxylic acids with tertiary amines could be carried out in the presence of the Ph3P-I2 activator. With an appropriate reagent addition sequence, a range of carboxylic acids including aliphatic, allylic, and aromatic acids could be converted into their corresponding tertiary amides under mild conditions without requirement of metal catalysis. | en_US |
| dc.subject | Chemical Engineering | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Metal-free amidation of carboxylic acids with tertiary amines | en_US |
| dc.type | Journal | en_US |
| article.title.sourcetitle | RSC Advances | en_US |
| article.volume | 6 | en_US |
| article.stream.affiliations | Chiang Mai University | en_US |
| Appears in Collections: | CMUL: Journal Articles | |
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