博碩士論文 102223027 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator陳致誠zh_TW
DC.creatorChih-Cheng Chenen_US
dc.date.accessioned2015-11-25T07:39:07Z
dc.date.available2015-11-25T07:39:07Z
dc.date.issued2015
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=102223027
dc.contributor.department化學學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract手性亞碸cis-2及trans-2可以透過市售的5-溴基戊酸乙酯為起始物,經過五步驟合成得到。我們應用這些手性亞碸催化劑進行二乙基鋅不對稱加成到苯甲醛反應上。我們也探討了酸添加劑在這個反應中如何促進催化過程。令人驚訝的是,當我們加入50 mol%的4-甲氧基苯甲酸(4-methoxybenzoic acid)時,發現產率和鏡像選擇性有明顯地改善。而且產物的絕對立體化學形式從S變成R。最後,我們也探討不同的芳香族醛進行二乙基鋅不對稱加成反應。zh_TW
dc.description.abstractChiral sulfoxide cis-2 and trans-2 were synthesized from commercially available 5-bromovalerate through a five-step synthetic route. We demonstrated the application of these chiral sulfoxide catalysts in asymmetric addition of diethylzinc to benzaldehyde and also investigated the promotion of the catalytic process by acid additives. Surprisingly, when we added 50 mol% of 4-methoxybenzoic acid, the yield and enantioselectivity were improved. In addition, the stereochemistry of product changed from S to R, Finally, We also investigated asymmetric addition of diethylzinc to different aromatic aldehydes.en_US
DC.subject亞碸zh_TW
DC.subject不對稱催化zh_TW
DC.subject二乙基鋅zh_TW
DC.subject乙基化zh_TW
DC.subjectsulfoxideen_US
DC.subjectasymmetric catalysisen_US
DC.subjectdiethylzincen_US
DC.subjectethylationen_US
DC.title以手性亞碸催化劑進行醛的不對稱乙基化反應之研究zh_TW
dc.language.isozh-TWzh-TW
DC.titleEnantioselective Ethylation of Aldehydes with Diethylzinc Catalyzed by Chiral Sulfoxideen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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