DC Field | Value | Language |
---|---|---|
dc.contributor.advisor | Han, Sunkyu | - |
dc.contributor.author | 강규민 | - |
dc.contributor.author | Kang, Gyumin | - |
dc.date.accessioned | 2024-08-08T19:31:54Z | - |
dc.date.available | 2024-08-08T19:31:54Z | - |
dc.date.issued | 2024 | - |
dc.identifier.uri | http://library.kaist.ac.kr/search/detail/view.do?bibCtrlNo=1100154&flag=dissertation | en_US |
dc.identifier.uri | http://hdl.handle.net/10203/322240 | - |
dc.description | 학위논문(박사) - 한국과학기술원 : 화학과, 2024.2,[v, 143 p. :] | - |
dc.description.abstract | Securinega alkaloids have captivated the synthetic community due to their high structural complexity, diversity, and potent bioactivities. While the synthesis of monomeric securinega alkaloid is well-established, the synthesis of their biosynthetic derivatives, including dimeric(oligomeric) securinega alkaloids and high-oxidation state derivatives, remains relatively underexplored due to their increased structural complexity. This dissertation encompasses the synthesis of high-oxidation state securinega alkaloids, fluvirosaones A, B, and secu′amamine A, flueggeacosine A, B, and suffranidine B. Synthesis of the aforementioned compounds, except secu′amamine A, were accomplished for the first time, by mimicking biosynthetic pathways or developing novel synthetic methodologies. | - |
dc.language | eng | - |
dc.publisher | 한국과학기술원 | - |
dc.subject | Securinega alkaloids▼aHigh-oxidation state securinega alkaloids▼aBiomimetic synthesis▼aBiosynthetic hypothesis▼aPhotocatalysis▼aCross-dehydrogenative coupling▼aNatural product synthesis | - |
dc.subject | 세큐리네가 알칼로이드▼a고산화준위 세큐리네가 알칼로이드▼a생체모방 합성▼a생합성 가설▼a광촉매▼a탈수소 교차 짝지음 반응▼a천연물 합성 | - |
dc.title | Synthesis of high-oxidation state securinega alkaloids | - |
dc.title.alternative | 고산화준위 세큐리네가 알칼로이드의 합성 | - |
dc.type | Thesis(Ph.D) | - |
dc.identifier.CNRN | 325007 | - |
dc.description.department | 한국과학기술원 :화학과, | - |
dc.contributor.alternativeauthor | 한순규 | - |
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