Publication: Total synthesis of 6-deoxyclitoriacetal isolated from Stemona collinsae Craib.
| dc.contributor.author | Prapas Khorphueng | en_US |
| dc.contributor.author | Jumreang Tummatorn | en_US |
| dc.contributor.author | Amorn Petsom | en_US |
| dc.contributor.author | Richard J.K. Taylor | en_US |
| dc.contributor.author | Sophon Roengsumran | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.contributor.other | University of York | en_US |
| dc.date.accessioned | 2018-08-20T06:50:24Z | |
| dc.date.available | 2018-08-20T06:50:24Z | |
| dc.date.issued | 2006-08-14 | en_US |
| dc.description.abstract | A total synthesis of the rotenoid, 6-deoxyclitoriacetal, a cytotoxic natural product, was successfully achieved by using platinum-catalysed hydroarylation, Sharpless asymmetric dihydroxylation, regioselective IBX diol oxidation and stereoselective intramolecular keto-aldehyde pinacol coupling as the key steps. © 2006 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.citation | Tetrahedron Letters. Vol.47, No.33 (2006), 5989-5991 | en_US |
| dc.identifier.doi | 10.1016/j.tetlet.2006.05.188 | en_US |
| dc.identifier.issn | 00404039 | en_US |
| dc.identifier.other | 2-s2.0-33745726167 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/22993 | |
| 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=33745726167&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 | Total synthesis of 6-deoxyclitoriacetal isolated from Stemona collinsae Craib. | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33745726167&origin=inward | en_US |