Publication: Synthesis of aryl α-keto esters via the rearrangement of aryl cyanohydrin carbonate esters
| dc.contributor.author | Nopporn Thasana | en_US |
| dc.contributor.author | Vilailak Prachyawarakorn | en_US |
| dc.contributor.author | Sopchok Tontoolarug | en_US |
| dc.contributor.author | Somsak Ruchirawat | en_US |
| dc.contributor.other | Chulabhorn Research Institute | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-07-24T03:21:05Z | |
| dc.date.available | 2018-07-24T03:21:05Z | |
| dc.date.issued | 2003-01-27 | en_US |
| dc.description.abstract | A facile synthesis of aryl α-keto esters is reported involving the rearrangement of aryl cyanohydrin carbonate esters induced by the α-carbanion to the nitrile group generated by LDA. However, under similar conditions, an o-benzyloxycyanohydrin carbonate ester rearranged via a domino reaction leading to 2-phenylbenzofuran-3-carboxylic acid. © 2003 Elsevier Science Ltd. All rights reserved. | en_US |
| dc.identifier.citation | Tetrahedron Letters. Vol.44, No.5 (2003), 1019-1021 | en_US |
| dc.identifier.doi | 10.1016/S0040-4039(02)02725-9 | en_US |
| dc.identifier.issn | 00404039 | en_US |
| dc.identifier.other | 2-s2.0-0037467813 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/20770 | |
| 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=0037467813&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 | Synthesis of aryl α-keto esters via the rearrangement of aryl cyanohydrin carbonate esters | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037467813&origin=inward | en_US |