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研究生: 鍾佑強
CHUNG YU-CHIANG
論文名稱: 高鏡像選擇性銠(I)/掌性雙烯配體催化芳香基硼酸對反丁烯二酸酯進行不對稱1,4加成反應及其合成應用 -α2腎上腺素受體拮抗劑全合成 -氮-苄基-3-苯基吡咯啶的不對稱合成
指導教授: 吳學亮
Wu, Hsyueh-Liang
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2011
畢業學年度: 99
語文別: 中文
論文頁數: 247
中文關鍵詞: 反丁烯二酸酯不對稱1,4-加成
英文關鍵詞: rhodium, fumarate, asymmetric 1,4-addition
論文種類: 學術論文
相關次數: 點閱:84下載:5
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  • 利用天然物左旋醋酸冰片酯49合成高穩定性的掌性雙環[2.2.1]雙烯配體,並結合銠(I)催化芳香基硼酸對反丁烯二酸酯進行不對稱1,4-加成反應。在這個催化系統中,銠(I) (1mol% of Rh)催化量和掌性雙烯配體進行不對稱1,4-加成反應,產物具有高產率和高立體選擇性(高達>99.5% ee值)。並將其應用在合成掌性3-(2-甲氧基)苯基吡咯啶(α2 -腎上腺素受體拮抗劑)和合成掌性氮-苄基-3-苯基吡咯啶。

    A new set of stable chiral bicyclo[2.2.1] diene ligands were prepared from (-)-bornyl acetate 49, and were employed in the rhodium(I)-catalyzed asymmetric 1,4-addition of arylboronic acids to fumarates. In this catalytic system, rhodium-diene complex (1.0 mol%) generated in situ from chiral diene 53a and [RhCl(C2H4)2]2 successfully yielded the corresponding adducts with good to excellent chemical yields and excellent levels of enantioselectivities (up to >99.5% ee). This methodology was demonstrated by its utilization in the enantioselective total synthesis of 3-(2-methoxyphenyl)pyrrolidine (an α2-adrenoceptor antagonist) and asymmetric synthesis of N-benzyl-3-phenylpyrrolidine.

    第一章 緒論..................... 1 第二章 文獻回顧................... 6 第三章 設計理念.................. . 15 第四章 實驗結果與討論................ 19 4-1 製備掌性[2.2.1]雙烯配體.............. 19 4-2 銠(I)金屬結合掌性配體催化不對稱 1,4-加成在 Fumaric 化合 物.......................... 20 4-2-1 改變加料順序及配位時間.............. 21 4-2-2、調整銠(I)催化量................. 23 4-2-3、改變配體上的芳香族官能基............ 24 4-2-4、溶劑效應................... 26 4-2-5、鹼效應..................... 28 4-2-6、最好條件下調整銠(I)催化量............ 29 4-2-7、底物例子(Substrate Scope) ............ 29 4-2-8、X-ray 繞射結構圖及預測立體化學路徑...... 32 第五章 合成與應用............... 36 5-1、前言.................... 36 5-2 文獻回顧................... 36 5-3、合成與應用................... 39 第六章 實驗步驟................. . 43 參考文獻....................... 93 附錄

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