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Oxidant-free, Iron-catalyzed Acceptorless Alcohol Dehydrogenation
DC Field | Value | Language |
---|---|---|
dc.contributor.advisor | Soon Hyeok Hong | - |
dc.contributor.author | 송한수 | - |
dc.date.accessioned | 2017-07-27T02:19:27Z | - |
dc.date.available | 2017-07-27T02:19:27Z | - |
dc.date.issued | 2014-08 | - |
dc.identifier.other | 000000021608 | - |
dc.identifier.uri | https://hdl.handle.net/10371/134911 | - |
dc.description | 학위논문 (석사)-- 서울대학교 대학원 : 화학부, 2014. 8. 홍순혁. | - |
dc.description.abstract | Oxidation of alcohols is an essential organic reaction, affording versatile carbonyl groups. To provide a sustainable solution for environmentally harmful traditional oxidation methods, the transition-metal catalyzed oxidant-free dehydrogenation of alcohols has attracted much attention. The widely used catalysts for the dehydrogenation reaction are based on precious metals, which are not economical and environmentally benign catalysts. We developed an operationally simple, economical, and environmentally benign acceptorless Fe-catalyzed dehydrogenation of various secondary benzylic alcohols to afford the corresponding ketones and H2. A simple in-situ mixture of readily available Fe(III) acetylacetonate, 1,10-phenanthroline, and K2CO3 was identified as an active catalyst for this transformation. | - |
dc.description.tableofcontents | Abstract 1
List of Tables 3 List of Figures 4 List of Schemes 4 Introduction 5 Results and Discussion 8 Conclusion 32 Experimental 33 1H NMR data for products 35 References 38 요약문 47 | - |
dc.format | application/pdf | - |
dc.format.extent | 594071 bytes | - |
dc.format.medium | application/pdf | - |
dc.language.iso | ko | - |
dc.publisher | 서울대학교 대학원 | - |
dc.subject | 철촉매 | - |
dc.subject.ddc | 540 | - |
dc.title | Oxidant-free, Iron-catalyzed Acceptorless Alcohol Dehydrogenation | - |
dc.type | Thesis | - |
dc.description.degree | Master | - |
dc.citation.pages | 45 | - |
dc.contributor.affiliation | 자연과학대학 화학부 | - |
dc.date.awarded | 2014-08 | - |
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