| DC 欄位 |
值 |
語言 |
| DC.contributor | 化學學系 | zh_TW |
| DC.creator | 管子萱 | zh_TW |
| DC.creator | kuan tzu-hsuan | en_US |
| dc.date.accessioned | 2021-8-30T07:39:07Z | |
| dc.date.available | 2021-8-30T07:39:07Z | |
| dc.date.issued | 2021 | |
| dc.identifier.uri | http://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=108223065 | |
| dc.contributor.department | 化學學系 | zh_TW |
| DC.description | 國立中央大學 | zh_TW |
| DC.description | National Central University | en_US |
| dc.description.abstract | 三甲基溴矽烷(bromotrimethylsilane)促進鄰芳乙炔基芐醇((oarylethynyl)
benzyl)生成溴取代的2-芳基苯乙酮(brominated 2-aryl
acetophenone)，並透過追蹤1H NMR 探討了其反應機制，此方法不含
金屬且操作簡單。
利用該方法我們製備了20 種不同的衍生物，其中產率最高可達
到99%，此外，我們還嘗試做了一些應用，進一步證明了該方法的實
用性。 | zh_TW |
| dc.description.abstract | A metal-free and operationally simple protocol has been developed to
prepare 2-Aryl acetophenone derivatives from readily available (o-
Arylethynyl)benzyl alcohols under an acid condition.
The reaction is scalable for 20 examples and the yields up to 99%,
further applications demonstrated the practicability of the protocol. | en_US |
| DC.subject | 方法學 | zh_TW |
| DC.title | 通過鄰芳乙炔基芐醇的氫溴化 和氧異構合成 2-芳基苯乙酮 | zh_TW |
| dc.language.iso | zh-TW | zh-TW |
| DC.type | 博碩士論文 | zh_TW |
| DC.type | thesis | en_US |
| DC.publisher | National Central University | en_US |