臺灣博碩士論文加值系統

在過去，手性胺基醇應用於Reformatsky的不對偁催化反應已經有相當初步的成果，1 而本論文是研究以本實驗室所開發的一系列雙手性胺基醇為掌性配位基，來進行Reformatsky的不對稱催化反應，由我們的實驗結果顯示，此類反應的產物之鏡像超越值可高達90%e.e。

The use of a series of chiral amino-alcohols as ligand to control the stereoselectivity of Reformatsky reaction has been examined. We found that, the β-hydroxy esters were prepared from asymmetric Reformatsky reactions with good enatioselectivity up to 90% e.e..

壹 、 摘要
貳 、 導論
參 、 結果與討論
肆 、 結論
伍 、 儀器測定及物質處理
陸 、 實驗步驟
柒 、 參考資料
捌 、 相關光譜

參考文獻（Reference）
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