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Synthesis of ChiraE Tridentate Ligands Embodying the Bispidine Framework and Their Application in the Enantioselective Addition of DiethyEzinc to Aldehydes

机译:肾小球三萜骨架的合成及其在对醛乙基乙基乙基乙烯的映选择性添加中的应用

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Several new chiral tridentate ligands with the bispidine moiety were synthesized from N-alkyl bispidines and chiral amino (or hydroxyl) acids. The synthesized ligands were used as catalysts in the enantioselective addition of diethylzinc to several aromatic aldehydes and an aliphatic aldehyde. High yield and enantioselectivity were received in the cases of aromatic aldehydes as substrates especially when the employed chiral ligand has a hydroxyl group attached to the chiral center. The effect of the structure, the amount of tridentate chiral ligands, solvent and temperature on the enantioselectivity of the addition products were studied. A possible mechanism for the addition of diethylzinc to aldehydes in the presence of bispidine-derived ligands were proposed based upon the catalytic reaction results and referred to the mechanisms proposed for other reaction systems in literatures.
机译:将具有Bispidine部分的几种新的手性三叉子配体由N-烷基哌啶氨酸和手性氨基(或羟基)酸合成。合成的配体用作对映选择性加入二乙基锌的催化剂,以几种芳香族醛和脂族醛。在芳香族醛的情况下,特别是当使用的手性配体具有连接到手性中心的羟基时,在芳族醛的情况下接收高产量和对映选择性。研究了该结构,三叉子手性配体,溶剂和温度对加成产物的对映选择性的影响。基于催化反应结果提出了在基于戊二啶衍生的配体存在下加入二乙基锌的可能机制,并提及所提出的文献中其他反应体系的机制。

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