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使用二苯甲酰基作为酰基源和手性酰基转移催化剂拆分外消旋 2-羟基酰胺的动力学拆分。

Kinetic Resolution of Racemic 2-Hydroxyamides Using a Diphenylacetyl Component as an Acyl Source and a Chiral Acyl-Transfer Catalyst.

机构信息

Department of Appliaed Chemistry, Faculty of Science, Tokyo University of Science, Tokyo 162-8601, Japan.

Graduate School of Natural Science and Technology, Shimane University, Shimane 690-8504, Japan.

出版信息

Molecules. 2018 Aug 10;23(8):2003. doi: 10.3390/molecules23082003.

Abstract

Various optically active 2-hydroxyamide derivatives are produced based on the kinetic resolution of racemic 2-hydroxyamides with a diphenylacetyl component and ()-benzotetramisole (()-BTM), a chiral acyl-transfer catalyst, via asymmetric esterification and acylation. It was revealed that a tertiary amide can be used with this novel protocol to achieve high selectivity (22 examples; -value reaching over 250). The resulting chiral compounds could be transformed into other useful structures while maintaining their chirality.

摘要

基于动力学拆分外消旋 2-羟基酰胺与手性酰基转移催化剂(-)-苯并四咪唑((-)-BTM)的反应,合成了各种光学活性的 2-羟基酰胺衍生物。通过不对称酯化和酰化反应。结果表明,该新方法可以使用叔酰胺实现高选择性(22 个实例;值超过 250)。得到的手性化合物可以在保持其手性的同时转化为其他有用的结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e4/6222459/9ce711ef6a5b/molecules-23-02003-sch001.jpg

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