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研究生: 阿努巴
Anupam Mukherjee
論文名稱: New Pathway Towards the Synthesis of Tetrabenzo[de,hi,mn,qr]naphthacenes bearing various Functionalities and Studies of their Photophysical and Electronic Properties & Transition Metal-Catalyzed Organic Transformations for the Synthesis of Functionalized Carbocyclic, Heterocyclic & Aminoalcohol Moieties
發展多取代 Tetrabenzo[de,hi,mn,qr]naphthacenes 化合物新的合成方法及其光物理和電子特性的研究及過渡金屬催化官能基化的碳環,雜環及氨基醇的合成。
指導教授: 劉瑞雄
Liu, Rai-Shung
口試委員: 沙晉康
蔡易州
侯敦仁
廖欣怡
陳銘洲
學位類別: 博士
Doctor
系所名稱: 理學院 - 化學系
Department of Chemistry
論文出版年: 2011
畢業學年度: 99
語文別: 英文
論文頁數: 465
中文關鍵詞: 金金屬催化環化反應鉑金屬
相關次數: 點閱:3下載:0
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  • 本篇論文探討含有烷基化tetrabenzo[de,hi,mn,qr]naphthacene化合物的合成及其光物理和電子特性的研究。過渡金屬催化有機分子行regiocontrolled hydrative carbocyclization及aminohydroxylation的反應,本篇論文共分成四個部份。

    第一章發表了利用1,2-di(phenanthren-4-yl)ethynes為起始物,合成有烷基化的tetrabenzo[de,hi,mn,qr]naphthacenes化合物,這是一個新的合成方法,我們也研究了不同烷基取代基的tetrabenzo[de,hi,mn,qr]naphthacenes化合物的光物理和電子特性,特別是HOMO-LOMO的能階,UV-吸收和螢光放光.

    第二章利用鉑金屬催化tethered alkynyl,nitrile enyones和enynals的環化反應,得到具有三環結構的產物。

    第三章探討使用o-(n-cyanoalkynyl)benzaldehydes為起始物合成出6-azaspiro[n+3, m+3]alkane的產物,此合成方法是經由三個步驟而得到。

    第四章利用金金屬催化aminoalkyne的起始物而得到2-aminoalcohols的產物,經由此反應路徑可得知nitrone在此反應中可將三鍵氧化而生成二胺基醇。


    Contents Page ACKNOWLEDGEMENTS iii ABSTRACT v LIST OF SCHEMES ix LIST OF TABLES xii LIST OF FIGURES xiii LIST OF PUBLICATIONS xv ABBREVIATIONS xvi CHAPTER 1: Functionalized Tetrabenzo[de,hi,mn,qr]naphthacene: A Convenient Synthesis and Variable Photophysical & Electronic properties Introduction 2 Results and Discussion 7 Conclusion 15 Experimental Procedures 16 Spectral Data of key compounds 20 References 28 CHAPTER 2: Pt-Catalyzed Chemoselective Hydrative Carbocyclization of Tethered Alkynyl and Nirile Enyones and Enynals : An Efficient Synthesis of Tricyclic Framework via A Sequential Oxo Assisted Hydration & Intramolecular Aldol Reaction Introduction 31 Results and Discussion 52 Conclusion 62 ii Experimental Procedures 62 Spectral Data of key compounds 74 References 91 CHAPTER 3: Synthesis of 6-azaspiro[n+3, m+3]alkane ring systems from o-(ncyanoalkynyl) benzaldehyde: A catalysis based three steps protocol Introduction 96 Results and Discussion 106 Conclusion 115 Experimental Procedures 116 Spectral Data of key compounds 117 References 127 CHAPTER 4: Gold-catalysed chemoselective synthesis of 2-aminoalcohols using aminoalkyne substrates Introduction 131 Results and Discussion 153 Conclusion 162 Experimental Procedures 163 Spectral Data of key compounds 166 References 185 X-RAY CRYSTAL DATA AND 1H & 13C NMR SPECTRA 191

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