Synthesis of tavacpallescensin and occidol via a common intermediate
| dc.citation.epage | 1210 | en_US |
| dc.citation.issue | 9 | en_US |
| dc.citation.spage | 1207 | en_US |
| dc.citation.volume | en_US | |
| dc.citation.woscount | 13 | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Lin, YJ | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:46:36Z | |
| dc.date.available | 2014-12-08T15:46:36Z | |
| dc.date.issued | 1999-05-07 | en_US |
| dc.description.abstract | The symmetrical benzosuberone 3 has been used in the synthesis of tavacpallescensin by an Emmons-Wadsworth condensation, selenium dioxide oxidation and diisobutylaluminium hydride reduction. For the elaboration of occidol, alpha-diazotization, Wolff rearrangement and reaction with methyllithium were involved. | en_US |
| dc.identifier.doi | 10.1039/a900465c | 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/a900465c | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/31343 | |
| dc.identifier.wosnumber | WOS:000080386000019 | |
| dc.language.iso | en_US | en_US |
| dc.title | Synthesis of tavacpallescensin and occidol via a common intermediate | en_US |
| dc.type | Article | en_US |