Synthesis of (-)-furodysinin from (+)-limonene
| dc.citation.epage | 1147 | en_US |
| dc.citation.issue | 10 | en_US |
| dc.citation.spage | 1147 | en_US |
| dc.citation.volume | en_US | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Chein, RJ | en_US |
| dc.contributor.department | 交大名義發表 | zh_TW |
| dc.contributor.department | 應用數學系 | zh_TW |
| dc.contributor.department | National Chiao Tung University | en_US |
| dc.contributor.department | Department of Applied Mathematics | en_US |
| dc.date.accessioned | 2014-12-08T15:02:38Z | |
| dc.date.available | 2014-12-08T15:02:38Z | |
| dc.date.issued | 1996-05-21 | en_US |
| dc.description.abstract | Furodysinin is synthesised by elaboration of (1R, 2R)-(+)-limonene oxide; key reactions include a tandem Claisen rearrangement-ene reaction and trapping of a conjugate adduct of an enone providing a bicyclic precursor of the sesquiterpene. | en_US |
| dc.identifier.doi | 10.1039/cc9960001147 | en_US |
| dc.identifier.issn | 1359-7345 | en_US |
| dc.identifier.journal | CHEMICAL COMMUNICATIONS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1039/cc9960001147 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/1287 | |
| dc.language.iso | en_US | en_US |
| dc.title | Synthesis of (-)-furodysinin from (+)-limonene | en_US |
| dc.type | Article | en_US |