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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Synthesis of a bipyridine-derived achiral thiourea trifluoromethanesulfonic acid salt and its application as an additive in organocatalytic asymmetric reactions
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Synthesis of a bipyridine-derived achiral thiourea trifluoromethanesulfonic acid salt and its application as an additive in organocatalytic asymmetric reactions

机译:联吡啶衍生的非手性硫脲三氟甲烷磺酸盐的合成及其在有机催化不对称反应中的应用

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摘要

The host-guest complex of a proline-thiourea bipyridine trifluoromethanesulfonic acid salt can catalyze organocatalytic asymmetric reactions such as aldol, Michael, and Mannich in polar protic medium with high stereoselectivities. The privileged bipyridine backbone and the thiourea motif are essential to the activity and enantioselectivity through hydrogen bonding interactions.
机译:脯氨酸-硫脲联吡啶三氟甲烷磺酸盐的主体-客体络合物可以在具有高立体选择性的极性质子介质中催化有机催化不对称反应,例如羟醛,迈克尔和曼尼希。优先的联吡啶骨架和硫脲基序对于通过氢键相互作用的活性和对映选择性至关重要。

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