Synthesis of cuparene and herbertene via a common intermediate
| dc.citation.epage | 2482 | en_US |
| dc.citation.issue | 17 | en_US |
| dc.citation.spage | 2479 | en_US |
| dc.citation.volume | en_US | |
| dc.citation.woscount | 22 | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Chang, MH | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:46:13Z | |
| dc.date.available | 2014-12-08T15:46:13Z | |
| dc.date.issued | 1999-09-07 | en_US |
| dc.description.abstract | A dihydroisobenzofuran (13) was obtained from beta-ionone in 10 steps via an intramolecular Diels-Alder reaction. On further oxidation, reductive ring opening and decarboxylation, cuparene and herbertene were synthesized. | en_US |
| dc.identifier.doi | 10.1039/a904068d | 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/a904068d | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/31092 | |
| dc.identifier.wosnumber | WOS:000082423200014 | |
| dc.language.iso | en_US | en_US |
| dc.title | Synthesis of cuparene and herbertene via a common intermediate | en_US |
| dc.type | Article | en_US |