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Pd(II) 催化的非手性 C(sp)-H 键的对映选择性分子内芳基化反应构建手性苯环化合物。

Pd(II)-Catalyzed Enantioselective Intramolecular Arylation of Unbiased C(sp)-H Bonds to Construct Chiral Benzo-ring Compounds.

机构信息

Department of Chemistry, Zhejiang University, Hangzhou 310027, China.

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, 529020, China.

出版信息

Org Lett. 2021 Jan 1;23(1):97-101. doi: 10.1021/acs.orglett.0c03775. Epub 2020 Dec 18.

Abstract

The asymmetric synthesis of chiral benzo-ring containing compounds through enantioselective intramolecular arylation of unbiased methylene C(sp)-H bonds was reported. Judicious choice of non-C-symmetric chiral phosphoric acid (CPA) ligand is crucial for the high reactivity and enantioselectivity. The slight decrease in enantioselectivity at the late stage of the reaction was attributed to the hydrolysis of CPA ligands to the corresponding BINOL.

摘要

通过非对映选择性的亚甲基 C(sp)-H 键的不对称分子内芳基化反应,实现了手性苯并环化合物的不对称合成。非手性磷酸(CPA)配体的合理选择对于高反应活性和对映选择性至关重要。在反应后期,对映选择性略有降低,这归因于 CPA 配体水解生成相应的 BINOL。

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