本論文旨在合成Hp-s1的類似物 NGLH-1並測試其生物活性。 在此,以D-lyxose為起始物,建構出植物鞘胺醇衍生物; 以D-glucose為起始物,建構出葡萄醣衍生物; 以N-Acetyl neuraminic acid為起始物,建構出唾液酸衍生物,之後將與實驗室同仁提供的化合物進行化學選擇性(chemoselective)醣苷化反應(glycosylation)及[1+1+2]的合成策略,目前已合成出主架構NGLH-1 (18-16)。
In this thesis, we purposed to synthesize neuritogenic ganglioside Hp-s1’s Analogues NGLH-1. In plan , we used D-lyxose to construct phytosphingosine; D-glucose to construct acceptor; N-Acetyl neuraminic acid to construct promoter, then use chemoselective glycosylation and [1+1+2] strategy. Now we have constructed our main structure NGLH-1(18-16) with the compound laboratory provided.