| DC 欄位 |
值 |
語言 |
| DC.contributor | 化學學系 | zh_TW |
| DC.creator | 蔡玫伶 | zh_TW |
| DC.creator | Mei-Ling Tsai | en_US |
| dc.date.accessioned | 2016-7-27T07:39:07Z | |
| dc.date.available | 2016-7-27T07:39:07Z | |
| dc.date.issued | 2016 | |
| dc.identifier.uri | http://ir.lib.ncu.edu.tw:444/thesis/view_etd.asp?URN=103223031 | |
| 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 | 以市售的5-溴基戊酸乙酯為起始物經由四步驟可以得到手性硫化物5a-c。另外，利用市售的苯并噻吩作為起始物，經由六步驟後合成具有光學活性的硫化物5d。硫化物5a-d 在三氯化鎵的幫助下合成出新穎的噁噻硼烷－氯化鎵錯合物18a-d，成功將其應用在不對稱Diels-Alder 催化反應得到不錯的產率及鏡像選擇性。 | zh_TW |
| dc.description.abstract | The chiral tetrahydrothiophene derivatives 5a-c were synthesized from commercially available 5-bromovalerate in 4 steps and the chiral dihydrobenzothiophene derivatives 5d was synthesized from commercially available benzothiophene in 6 steps. We successfully synthesized a novel oxathiaborolium using gallium trichloride as the halophile, and successfully applied it in catalystic and asymmetric Diels-Alder reactionin excellent yield with high stereoselectivity. | en_US |
| DC.subject | Diels-Alder反應 | zh_TW |
| DC.subject | 噁噻硼烷 | zh_TW |
| DC.title | 噁噻硼烷－氯化鎵錯合物催化不對稱 Diels-Alder 反應之研究 | zh_TW |
| dc.language.iso | zh-TW | zh-TW |
| DC.title | Oxathiaborolium Gallium Chloride Complexes Catalyzed Asymmetric Diels-Alder Reactions | en_US |
| DC.type | 博碩士論文 | zh_TW |
| DC.type | thesis | en_US |
| DC.publisher | National Central University | en_US |