SYNTHETIC STUDIES TOWARDS FAVELINE METHYL-ETHER
| dc.citation.epage | 5824 | en_US |
| dc.citation.issue | 20 | en_US |
| dc.citation.spage | 5819 | en_US |
| dc.citation.volume | 51 | en_US |
| dc.citation.woscount | 4 | |
| dc.contributor.author | HO, TL | en_US |
| dc.contributor.author | CHEN, CK | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:03:22Z | |
| dc.date.available | 2014-12-08T15:03:22Z | |
| dc.date.issued | 1995-05-15 | en_US |
| dc.description.abstract | A convergent approach to faveline methyl ether based on Claisen rearrangement is delineated Thus the benzylic and allylic alcohol substrate was assembled by a Grignard reaction, and the rearrangement product was oxidized and cyclized. Double bond isomers of faveline methyl ether were obtained. | en_US |
| dc.identifier.doi | 10.1016/0040-4020(95)00240-9 | en_US |
| dc.identifier.issn | 0040-4020 | en_US |
| dc.identifier.journal | TETRAHEDRON | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/0040-4020(95)00240-9 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/1917 | |
| dc.identifier.wosnumber | WOS:A1995QY11200010 | |
| dc.language.iso | en_US | en_US |
| dc.title | SYNTHETIC STUDIES TOWARDS FAVELINE METHYL-ETHER | en_US |
| dc.type | Article | en_US |