Synthesis of elvirol methyl ether
| dc.citation.epage | 881 | en_US |
| dc.citation.issue | 5 | en_US |
| dc.citation.spage | 879 | en_US |
| dc.citation.volume | 48 | en_US |
| dc.citation.woscount | 3 | |
| 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 | 2014-12-08T15:43:21Z | |
| dc.date.available | 2014-12-08T15:43:21Z | |
| dc.date.issued | 2001-10-01 | en_US |
| dc.description.abstract | Elvirol methyl ether has been synthesized from p-cresol via 2-(2-cyclopentenyl)-4-methylphenyl methyl ether by ozonolysis, dithioacetalization, reduction, and Wittig reaction. The overall yield was 18.8%. | en_US |
| dc.identifier.issn | 0009-4536 | en_US |
| dc.identifier.journal | JOURNAL OF THE CHINESE CHEMICAL SOCIETY | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/29349 | |
| dc.identifier.wosnumber | WOS:000172519800009 | |
| dc.language.iso | en_US | en_US |
| dc.subject | sesquiterpenes | en_US |
| dc.subject | ozonolysis | en_US |
| dc.subject | Wittig reaction | en_US |
| dc.subject | elvirol methyl ether | en_US |
| dc.title | Synthesis of elvirol methyl ether | en_US |
| dc.type | Article | en_US |
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