DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, Wonchul | ko |
dc.contributor.author | Youn, Joo-Hack | ko |
dc.contributor.author | Kang, SungHo | ko |
dc.date.accessioned | 2013-08-08T06:06:53Z | - |
dc.date.available | 2013-08-08T06:06:53Z | - |
dc.date.created | 2013-06-24 | - |
dc.date.created | 2013-06-24 | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | CHEMICAL COMMUNICATIONS, v.49, no.45, pp.5231 - 5233 | - |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.uri | http://hdl.handle.net/10203/174924 | - |
dc.description.abstract | (-)-Kaitocephalin has been synthesized. With the C9 stereocenter from Garner's aldehyde, the C4 quaternary carbon was installed by the desymmetrization of the Cbz-protected serinol. The remaining stereogenic centers were generated through mercuriocyclization, epoxidation and regioselective epoxide opening, in which the quaternary carbon most likely played crucial roles in the stereoinduction. | - |
dc.language | English | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.subject | RECEPTOR ANTAGONIST | - |
dc.subject | KAITOCEPHALIN | - |
dc.subject | ALCOHOLS | - |
dc.subject | REVISION | - |
dc.subject | ACID | - |
dc.title | Total synthesis of (-)-kaitocephalin | - |
dc.type | Article | - |
dc.identifier.wosid | 000318790500035 | - |
dc.identifier.scopusid | 2-s2.0-84877840225 | - |
dc.type.rims | ART | - |
dc.citation.volume | 49 | - |
dc.citation.issue | 45 | - |
dc.citation.beginningpage | 5231 | - |
dc.citation.endingpage | 5233 | - |
dc.citation.publicationname | CHEMICAL COMMUNICATIONS | - |
dc.identifier.doi | 10.1039/c3cc42365d | - |
dc.contributor.localauthor | Kang, SungHo | - |
dc.contributor.nonIdAuthor | Lee, Wonchul | - |
dc.contributor.nonIdAuthor | Youn, Joo-Hack | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | RECEPTOR ANTAGONIST | - |
dc.subject.keywordPlus | KAITOCEPHALIN | - |
dc.subject.keywordPlus | ALCOHOLS | - |
dc.subject.keywordPlus | REVISION | - |
dc.subject.keywordPlus | ACID | - |
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