A synthesis of 6-myoporol
| dc.citation.epage | 494 | en_US |
| dc.citation.spage | 493 | en_US |
| dc.citation.volume | 60 | en_US |
| dc.citation.woscount | 2 | en_US |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Chein, RJ | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2019-04-02T06:00:02Z | |
| dc.date.available | 2019-04-02T06:00:02Z | |
| dc.date.issued | 1997-05-01 | en_US |
| dc.description.abstract | An approach to (+/-)-6-myoporol (1) featured stereocontrol by equilibration of 2,6-disubstituted cyclohexanones to mainly the cis isomer. The synthesis was completed by reaction of a lactone intermediate with 3-lithiofuran, Mitsunobu reaction, and hydrolysis. | en_US |
| dc.identifier.doi | 10.1021/np960704f | en_US |
| dc.identifier.issn | 0163-3864 | en_US |
| dc.identifier.journal | JOURNAL OF NATURAL PRODUCTS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1021/np960704f | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/149528 | |
| dc.identifier.wosnumber | WOS:A1997XA68500017 | en_US |
| dc.language.iso | en_US | en_US |
| dc.title | A synthesis of 6-myoporol | en_US |
| dc.type | Article | en_US |
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