Publication: Hexabromoacetone and ethyl tribromoacetate: a highly efficient reagent for bromination of alcohol
| dc.contributor.author | Pratoomrat Tongkate | en_US |
| dc.contributor.author | Wanchai Pluempanupat | en_US |
| dc.contributor.author | Warinthorn Chavasiri | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-07-12T02:19:45Z | |
| dc.date.available | 2018-07-12T02:19:45Z | |
| dc.date.issued | 2008-02-11 | en_US |
| dc.description.abstract | A new and efficient method for the bromination of alcohols utilizing Br3CCOCBr3/PPh3and Br3CCO2Et/PPh3is described. Various alcohols can be converted smoothly into their corresponding alkyl bromides in high yields under mild conditions with short reaction times. Based upon1H NMR studies using competitive reactions between selected brominating agents and Cl3CCN, Br3CCOCBr3displays the highest reactivity approximately nine times that of CBr4. © 2007 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.citation | Tetrahedron Letters. Vol.49, No.7 (2008), 1146-1148 | en_US |
| dc.identifier.doi | 10.1016/j.tetlet.2007.12.061 | en_US |
| dc.identifier.issn | 00404039 | en_US |
| dc.identifier.other | 2-s2.0-38349022154 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/18970 | |
| dc.rights | Mahidol University | en_US |
| dc.rights.holder | SCOPUS | en_US |
| dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=38349022154&origin=inward | 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 | Hexabromoacetone and ethyl tribromoacetate: a highly efficient reagent for bromination of alcohol | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=38349022154&origin=inward | en_US |