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- Kee, Jung-Min
- Bioorganic and Chembio Lab.
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| DC Field | Value | Language |
|---|---|---|
| dc.citation.endPage | 5376 | - |
| dc.citation.number | 23 | - |
| dc.citation.startPage | 5373 | - |
| dc.citation.title | ORGANIC LETTERS | - |
| dc.citation.volume | 8 | - |
| dc.contributor.author | Wender, Paul A. | - |
| dc.contributor.author | Bi, F. Christopher | - |
| dc.contributor.author | Buschmann, Nicole | - |
| dc.contributor.author | Gosselin, Francis | - |
| dc.contributor.author | Kan, Cindy | - |
| dc.contributor.author | Kee, Jung-Min | - |
| dc.contributor.author | Ohmura, Hirofumi | - |
| dc.date.accessioned | 2023-12-22T09:40:15Z | - |
| dc.date.available | 2023-12-22T09:40:15Z | - |
| dc.date.created | 2015-08-04 | - |
| dc.date.issued | 2006-11 | - |
| dc.description.abstract | [GRAPHICS] 12-Hydroxydaphnetoxins, members of the structurally fascinating daphnane diterpene family, exhibit a wide range of significant biological activities. A general route to the BC-ring system of 12-hydroxy daphnetoxins is reported based on D-ribose. Depending on the choice of protecting groups and solvent, the oxidopyrylium-alkene [5+2] cycloaddition originating from A provides cycloadduct diastereomer B or C with good to excellent selectivity | - |
| dc.identifier.bibliographicCitation | ORGANIC LETTERS, v.8, no.23, pp.5373 - 5376 | - |
| dc.identifier.doi | 10.1021/ol062234e | - |
| dc.identifier.issn | 1523-7060 | - |
| dc.identifier.scopusid | 2-s2.0-33845236874 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/13351 | - |
| dc.identifier.url | http://pubs.acs.org/doi/abs/10.1021/ol062234e | - |
| dc.identifier.wosid | 000241729500050 | - |
| dc.language | 영어 | - |
| dc.publisher | AMER CHEMICAL SOC | - |
| dc.title.alternative | Studies on oxidopyrylium [5+2] cycloadditions: Toward a general syntheti c route to the C12-hydroxy daphnetoxins | - |
| dc.title | Studies on oxidopyrylium [5+2] cycloadditions: Toward a general synthetic route to the C12-hydroxy daphnetoxins | - |
| dc.type | Article | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.subject.keywordPlus | ENANTIOPURE | - |
| dc.subject.keywordPlus | DITERPENE | - |
| dc.subject.keywordPlus | DAPHNANE | - |
| dc.subject.keywordPlus | PHORBOL | - |
| dc.subject.keywordPlus | (+)-RESINIFERATOXIN | - |
| dc.subject.keywordPlus | TUMOR PROMOTERS | - |
| dc.subject.keywordPlus | STEREOSELECTIVE-SYNTHESIS | - |
| dc.subject.keywordPlus | ASYMMETRIC INDUCTION | - |
| dc.subject.keywordPlus | ALDOL REACTIONS | - |
| dc.subject.keywordPlus | RING | - |
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