The thiazolidine ligands with aromatic substituents on C-2 position provided relatively poor enantioselectivity .

而C-2位芳基取代的 噻唑 烷 酸 及 醇配体的 催化 性能 则略差。

Synthesis of sugar derivatives of thiazolidine 4 carboxylic acid and primary research of its antitumor activity

壳 寡糖，氨基 葡萄糖及其衍生物的 抗氧化功能研究 硫 杂 脯氨酸糖衍生物的合成及其抗肿瘤活性初步探讨

Studies on the Chiral Structure of Thiazolidine Ligands and Their Application to Asymmetric Hydrosilylation of Acetophenone

噻唑 烷类配体的手性结构及其在催化苯乙酮不对称硅氢化反应中的应用研究

It was sound that the configuration of C2 in thiazolidine had no effect on the catalytic reaction .

e. 左右， 噻唑 烷 环上的C2构型对催化反应 结果无影响，C 4 位上 酯基的影响也不大。

We also studied the asymmetric borane reduction of prochiral ketone catalyzed by a series of thiazolidine ligands .

本文考察了由L- 半胱氨酸 衍生 的 2-位无 取 代基 的 以及 2-位芳基取代的 噻唑烷酸及 醇配体在前手性酮的不对称还原反应中的催化性能。

Review of the therapeutic effect of thiazolidine treating for diabetes mellitus type ⅱ

噻唑 烷 二 酮类 药物治疗2型糖尿病的效果