藉由鈀催化Heck醣苷化反應進行Pseudouridine的合成研究

dc.contributor簡敦誠zh_TW
dc.contributorChien, Tun-Chengen_US
dc.contributor.author張馨云zh_TW
dc.contributor.authorChang, Hsin-Yunen_US
dc.date.accessioned2019-09-04T09:07:35Z
dc.date.available不公開
dc.date.available2019-09-04T09:07:35Z
dc.date.issued2016
dc.description.abstractC-nucleosides相較於N-nucleosides擁有較穩定的醣苷鍵,在醫藥化學及生物化學上具有應用的潛力。且在自然界中,存在許多C-nucleosides的天然物,具有多樣的生物活性,其中天然物pseudouridine及其衍生物2’-deoxypseudouridine為我們有興趣的化合物。本研究主要著重於利用Heck反應將醣體和具有碘取代的芳香及雜環化合物進行耦合,形成新的碳-碳醣苷鍵。改變以往需要使用到有毒且而昂貴的AsPh3作為配體,以雙芽基配體作為配體進行反應,發現也有很好的區位及立體選擇性。並將研究結果應用於2’-deoxypseudouridine及pseudouridine的合成。zh_TW
dc.description.abstractThe nucleosidic bond of C-nucleosides are much more stable than N-nucleosides, which allows potential applications of C-nucleosides in medi-cinal chemistry and chemical biology. Some of the naturally occurring C-nucleosides possess a wide variety of biological activities. We are particu-larly interested in the synthesis of pseudouridine and 2’-deoxypseudouridine. In this thesis, we employed Heck-type coupling reactions to form C-C bonds between the anomeric carbon of 1, 2-unhydrous sugar derivatives and aryl iodides or iodo-heterocycles. Instead of utilizing toxic and expensive AsPh3 as the ligand, tour study has showed that the use of bidentate ligands for Heck-type coupling reactions were highly regio- and stereoselective. The methodology is applicable to the synthesis of 2’-deoxypseudouridine and pseudouridine.en_US
dc.description.sponsorship化學系zh_TW
dc.identifierG060342060S
dc.identifier.urihttp://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22G060342060S%22.&%22.id.&
dc.identifier.urihttp://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100067
dc.language中文
dc.subjectC-核苷zh_TW
dc.subject類尿嘧啶zh_TW
dc.subject2’-脫氧類尿嘧啶zh_TW
dc.subjectHeck反應zh_TW
dc.subjectC-nucleosideeen_US
dc.subjectpseudouridinen_US
dc.subject2’-deoxypseudouridineen_US
dc.subjectHeck reactionen_US
dc.title藉由鈀催化Heck醣苷化反應進行Pseudouridine的合成研究zh_TW
dc.titleSynthetic Studies of Pseudouridine via Palladium-catalyzed Heck-type Glycosylation Reactionen_US

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