A new and concise synthetic route to an enantiopure (+)-conduritol-E derivative from diethyl L-tartrate
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, WW | ko |
| dc.contributor.author | Chang, Sukbok | ko |
| dc.date.accessioned | 2013-02-27T13:13:00Z | - |
| dc.date.available | 2013-02-27T13:13:00Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1999-12 | - |
| dc.identifier.citation | TETRAHEDRON-ASYMMETRY, v.10, no.23, pp.4473 - 4475 | - |
| dc.identifier.issn | 0957-4166 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/68775 | - |
| dc.description.abstract | (+)-(1R,2R,3S,6S)-3,6-Di-O-methyl conduritol-E was efficiently synthesized in enantiomerically pure form starting from diethyl L-tartrate in 33% total yield using a ring-closing olefin metathesis reaction as one of the key steps. (C) 1999 Published by Elsevier Science Ltd. All rights reserved. | - |
| dc.language | English | - |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
| dc.subject | RING-CLOSING METATHESIS | - |
| dc.subject | OLEFIN METATHESIS | - |
| dc.subject | ORGANIC-SYNTHESIS | - |
| dc.subject | INHIBITORS | - |
| dc.subject | ALCOHOLS | - |
| dc.subject | ACID | - |
| dc.title | A new and concise synthetic route to an enantiopure (+)-conduritol-E derivative from diethyl L-tartrate | - |
| dc.type | Article | - |
| dc.identifier.wosid | 000084665600003 | - |
| dc.identifier.scopusid | 2-s2.0-0033367403 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 10 | - |
| dc.citation.issue | 23 | - |
| dc.citation.beginningpage | 4473 | - |
| dc.citation.endingpage | 4475 | - |
| dc.citation.publicationname | TETRAHEDRON-ASYMMETRY | - |
| dc.identifier.doi | 10.1016/S0957-4166(99)00517-0 | - |
| dc.contributor.localauthor | Chang, Sukbok | - |
| dc.contributor.nonIdAuthor | Lee, WW | - |
| dc.type.journalArticle | Article | - |
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