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首页> 外文期刊>The Journal of Organic Chemistry >A chemoenzymatic dynamic kinetic resolution approach to enantiomerically pure (R)- and (S)-duloxetine
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A chemoenzymatic dynamic kinetic resolution approach to enantiomerically pure (R)- and (S)-duloxetine

机译:对映体纯的(R)-和(S)-度洛西汀的化学酶动力学动力学拆分方法

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摘要

The synthesis of (R)-duloxetine is described. Dynamic kinetic resolution of β-hydroxynitrile rac-1 using Candida antarctica lipase B (CALB, N435) and ruthenium catalyst 6 afforded β-cyano acetate (R)-2 in high yield and in excellent enantioselectivity (98% ee). The subsequent synthetic steps were straightforward and (R)-duloxetine was isolated in 37% overall yield over 6 steps. The synthetic route also constitute a formal total synthesis of (S)-duloxetine.
机译:描述了(R)-度洛西汀的合成。使用南极假丝酵母脂肪酶B(CALB,N435)和钌催化剂6动力学拆分β-羟基腈rac-1,可以高收率和出色的对映选择性(98%ee)获得β-氰基乙酸酯(R)-2。随后的合成步骤很简单,在6个步骤中,以37%的总收率分离了(R)-度洛西汀。合成途径也构成了(S)-度洛西汀的正式全合成。

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