DC Field | Value | Language |
---|---|---|
dc.contributor.advisor | Park, Ho-Koon | - |
dc.contributor.advisor | 박호군 | - |
dc.contributor.author | Shin, Hyun-Ik | - |
dc.contributor.author | 신현익 | - |
dc.date.accessioned | 2011-12-13T04:56:12Z | - |
dc.date.available | 2011-12-13T04:56:12Z | - |
dc.date.issued | 1985 | - |
dc.identifier.uri | http://library.kaist.ac.kr/search/detail/view.do?bibCtrlNo=64384&flag=dissertation | - |
dc.identifier.uri | http://hdl.handle.net/10203/32418 | - |
dc.description | 학위논문(석사) - 한국과학기술원 : 화학과, 1985.2, [ [iii], 52 p. ] | - |
dc.description.abstract | The naturally occuring sesquiterpene known as eudesmol has been synthesized from R-(+)-limonene in ten steps using intramolecular Diels-Alder reaction as a key step. Tetraene was prepared from R-(+)-limonene in five steps, by a sequence of epoxidation, hydrolysis, oxidative cleavage, and two consecutive Wittig reactions. Octalin, a product of intramolecular Diels-Alder reaction of tetraene, could be converted to $\alpha$-, or $\beta$-eudesmol by a series of reactions; epoxidation, reduction, oxidation, followed by Shapiro or Wittig reaction. ## | eng |
dc.language | eng | - |
dc.publisher | 한국과학기술원 | - |
dc.title | Total synthesis of eudesmol via an intramolecular diels-alder reaction | - |
dc.title.alternative | 분자내 디일스-알더 반응을 이용한 유데스몰의 전 합성 | - |
dc.type | Thesis(Master) | - |
dc.identifier.CNRN | 64384/325007 | - |
dc.description.department | 한국과학기술원 : 화학과, | - |
dc.identifier.uid | 000831568 | - |
dc.contributor.localauthor | Park, Ho-Koon | - |
dc.contributor.localauthor | 박호군 | - |
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