博碩士論文 942203008 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator孫崇喜zh_TW
DC.creatorChong-si Sunen_US
dc.date.accessioned2007-7-21T07:39:07Z
dc.date.available2007-7-21T07:39:07Z
dc.date.issued2007
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=942203008
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本論文提供「環閉合置換反應(ring closing metathesis, RCM)後產生之烯烴進行選擇性衍生化的方法」,並藉由鈀金屬催化甲酸還原反應(palladium catalyzed formate reduction)來達成此一目的。我們使用二氫吡喃(dihydropyrane)雜環 4 為模型,以改變甲酸還原反應之配位基的方式,尋找適用於環閉合置換後的含氧六員雜環進行甲基烯衍生之最佳條件。 為了探討此方法於有機合成上的實用性,我們更進一步地合成了4-及5-取代哌啶甲酸(pipecolic acid)的前驅物 28a、29、35、36 及 38。其關鍵步驟在於「環閉合置換反應來組成哌啶甲酸六員雜環的基本骨架,並串聯鈀金屬催化甲酸還原反應進行甲基烯衍生」;而哌啶甲酸2 號位置上的掌性中心,則藉由 Dellaria 教授的「光學輔助胺基乙酸烯醇合成子之立體選擇烷化反應stereoselective alkylation)」及 Royer、Husson 團隊的「去質子/光學輔助立體選擇質子化反應」進行不對稱合成的控制。zh_TW
dc.description.abstractThe method for regioselective palladium-catalyzed formate reduction of allylic benzoate formed by ring closing metathesis was developed. We used 2,2-diphenyl-tetrahydro-2H- pyrane 4 as the model compound, and found an optimized condition of formate reduction by screening several ligands. 4- or 5-Substituted pipecolic acid precursors 28a, 29, 35, 36 and 38, which are biologically active compounds or their precursors, were synthesized by this method. The key steps of these syntheses involve the formation of the skeleton of pipecolic acids with ring closing metathesis and transformation of endo-olefins with palladium-catalyzed formate reduction. We used stereoselective alkylation and deprotonation/stereoselective protonation to control the generation of chiral center in these pipecolic acid precursors.en_US
DC.subject環閉合置換zh_TW
DC.subject鈀催化甲酸還原zh_TW
DC.subject酮基哌啶甲酸zh_TW
DC.subjectOxopipecolic aciden_US
DC.subjectRing closing metathesisen_US
DC.subjectPalladium-catalyzed formate reductionen_US
DC.title利用鈀催化還原異構與烯醇丙烯化反應不對稱合成4-及5-取代哌啶甲酸衍生物zh_TW
dc.language.isozh-TWzh-TW
DC.titleAsymmetric Synthesis of 4- or 5-Oxopipecolic Acid Derivatives via Palladium-Catalyzed Formate Reduction and Enolate Allylation.en_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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