手性2-(2-吡啶基)-4-羧乙基-1, 3-噻唑烷的合成及应用研究 |
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引用本文: | 姚金水,刘丹凤,李弘,何炳林.手性2-(2-吡啶基)-4-羧乙基-1, 3-噻唑烷的合成及应用研究[J].有机化学,1998,18(4):372-376. |
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作者姓名: | 姚金水 刘丹凤 李弘 何炳林 |
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作者单位: | 山东轻工业学院化学工程系 |
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摘 要: | 以分级结晶和柱层析法对手性配体2-(2-吡啶基)-4-羧乙基-1,3-噻唑烷(A)进行了异构体分离提纯。将其与Rh(COD)Cl]~2制备的原位催化剂用于催化苯乙酮及其它几种芳香酮的不对称硅氢化反应, 化学收率达90%左右, 光学纯度达80%e.e.左右, 噻唑烷环上的C~2构型对催化反应结果无影响, C~4位上酯基的影响也不大。
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关 键 词: | 合成 苯乙酮 乙基 异构体 芳香族化合物 羧基 噻唑烷 P 酮 P 手性试剂 催化活性 |
Study on synthesis and application of 2-(2-pyridyl)-4-carboethoxy-1, 3-thiazolidine |
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Abstract: | The isomers of ligand, 2-(2-pyridyl)-4-carboethoxy- 1,3-thiazolidine(A) were separated and purified by fractional crystallization or column chromatography. The catalysts, prepared in-situ with ligand A and Rh(COD)Cl]~2, were used to catalyze the asymmetric hydrosilylation of acetophenone and several other aromatic ketones. The chemical yields and optical purities were about 90% and 80%, respectively. It was sound that the configuration of C~2 in thiazolidine had no effect on the catalytic reaction. |
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Keywords: | SYNTHESIS ACETOPHENONE ETHYL GROUP ISOMER AROMATIC COMPOUNDS CARBOXY GROUP THIAZOLIDINE P KETONE P CHIRAL REAGENT CATALYTIC ACTIVITY |
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