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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Subin Jaita | en_US |
dc.contributor.author | Pantitra Kaewkum | en_US |
dc.contributor.author | Chuthamat Duangkamol | en_US |
dc.contributor.author | Wong Phakhodee | en_US |
dc.contributor.author | Mookda Pattarawarapan | en_US |
dc.date.accessioned | 2018-09-04T09:47:04Z | - |
dc.date.available | 2018-09-04T09:47:04Z | - |
dc.date.issued | 2014-01-01 | en_US |
dc.identifier.issn | 20462069 | en_US |
dc.identifier.other | 2-s2.0-84907647139 | en_US |
dc.identifier.other | 10.1039/c4ra08643k | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907647139&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/53329 | - |
dc.description.abstract | © the Partner Organisations 2014. A simple, rapid, and eco-friendly method for NaBH4 reduction of carboxylic acids to alcohols under solvent-free conditions was developed using a combination of 2,4,6-trichloro-1,3,5-triazine (TCT) with a catalytic amount of triphenylphosphine as an acid activator. With the 1 : 0.2 : 1.5 : 2 mole ratio of TCT : PPh3 : K2CO3 : NaBH4, carboxylic acids including aromatic acids, aliphatic acids, and N-protected α-amino acids (Fmoc, Z) could readily undergo reduction to give the corresponding alcohols in good to excellent yields within 10 min. | en_US |
dc.subject | Chemical Engineering | en_US |
dc.subject | Chemistry | en_US |
dc.title | Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | RSC Advances | en_US |
article.volume | 4 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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