Publication: Asymmetric total synthesis of (+)-swainsonine
| dc.contributor.author | Soontorn Chooprayoon | en_US |
| dc.contributor.author | Chutima Kuhakarn | en_US |
| dc.contributor.author | Patoomratana Tuchinda | en_US |
| dc.contributor.author | Vichai Reutrakul | en_US |
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-05-03T08:04:14Z | |
| dc.date.available | 2018-05-03T08:04:14Z | |
| dc.date.issued | 2011-01-21 | en_US |
| dc.description.abstract | A concise asymmetric synthesis of (+)-swainsonine (ent-1) is described starting from 2, which was readily prepared from commercially available l-glutamic acid. The method features installation of the indolizidine ring via an intramolecular cyclisation of α-sulfinyl carbanion as a key step. (+)-Swainsonine was obtained in 11.8% overall yield in 10 steps. © 2011 The Royal Society of Chemistry. | en_US |
| dc.identifier.citation | Organic and Biomolecular Chemistry. Vol.9, No.2 (2011), 531-537 | en_US |
| dc.identifier.doi | 10.1039/c0ob00388c | en_US |
| dc.identifier.issn | 14770520 | en_US |
| dc.identifier.other | 2-s2.0-78650732491 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/11603 | |
| 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=78650732491&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Asymmetric total synthesis of (+)-swainsonine | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650732491&origin=inward | en_US |