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有机催化对映选择性邻羟基芳基酮与三氟甲基酮的交叉Aldol 反应。

Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones.

机构信息

Institute of Biochemistry and Molecular Biology, School of Life Sciences, Lanzhou University , Lanzhou 730000, China.

State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.

出版信息

Org Lett. 2017 May 19;19(10):2634-2637. doi: 10.1021/acs.orglett.7b00828. Epub 2017 May 8.

Abstract

The enantioselective cross-aldol reaction between o-hydroxyacetophenones and trifluoromethyl ketones catalyzed by chiral thiourea organocatalysts is reported. Gram-scale synthesis of the cross-aldol product was carried out, with no decrease in the yield and enantioselectivity. Furthermore, the cross-aldol products thus prepared were used in the preparation of medicinally interesting 3,5-diaryl-5-trifluoromethyl-2-isoxazoline and β-trifluoromethyl-β-tertiary hydroxy acid ester with high yield and enantiopurity.

摘要

报告了手性硫脲有机催化剂催化邻羟基苯乙酮与三氟甲基酮的对映选择性交叉羟醛缩合反应。进行了克级规模的交叉羟醛缩合产物合成,产率和对映选择性没有降低。此外,由此制备的交叉羟醛缩合产物还用于高收率和对映纯度地制备具有药用价值的 3,5-二芳基-5-三氟甲基-2-异恶唑啉和β-三氟甲基-β-叔羟基酸酯。

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