簡敦誠Chien, Tun-Cheng張馨云Chang, Hsin-Yun2019-09-04不公開2019-09-042016http://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22G060342060S%22.&%22.id.&http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100067C-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。The 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.C-核苷類尿嘧啶2’-脫氧類尿嘧啶Heck反應C-nucleosideepseudouridin2’-deoxypseudouridineHeck reaction