A stereoselective synthesis of platyphyllide
| dc.citation.epage | 1826 | en_US |
| dc.citation.issue | 13 | en_US |
| dc.citation.spage | 1823 | en_US |
| dc.citation.volume | en_US | |
| dc.citation.woscount | 10 | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Ho, MF | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:46:23Z | |
| dc.date.available | 2014-12-08T15:46:23Z | |
| dc.date.issued | 1999-07-07 | en_US |
| dc.description.abstract | The norsesquiterpene lactone, platyphyllide has been synthesized in 8 steps in 23% overall yield via the Diels-Alder adduct of 2-(4-methylpent-3-enyl)furan with dimethyl acetylenedicarboxylate, the 3-substituted phthalic diester, and an o-formylbenzamide. An intramolecular ene reaction established the skeleton, and the final step involved inversion of configuration at the benzylic site. | en_US |
| dc.identifier.doi | 10.1039/a902410g | en_US |
| dc.identifier.issn | 0300-922X | en_US |
| dc.identifier.journal | JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1039/a902410g | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/31211 | |
| dc.identifier.wosnumber | WOS:000081549700007 | |
| dc.language.iso | en_US | en_US |
| dc.title | A stereoselective synthesis of platyphyllide | en_US |
| dc.type | Article | en_US |