Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/53329
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSubin Jaitaen_US
dc.contributor.authorPantitra Kaewkumen_US
dc.contributor.authorChuthamat Duangkamolen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-04T09:47:04Z-
dc.date.available2018-09-04T09:47:04Z-
dc.date.issued2014-01-01en_US
dc.identifier.issn20462069en_US
dc.identifier.other2-s2.0-84907647139en_US
dc.identifier.other10.1039/c4ra08643ken_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907647139&origin=inwarden_US
dc.identifier.urihttp://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.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleSolvent-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.typeJournalen_US
article.title.sourcetitleRSC Advancesen_US
article.volume4en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.