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联萘酚脯氨醇手性配体:设计及其在手性芳醛的不对称芳基化反应中的应用。

Binaphthyl-prolinol chiral ligands: design and their application in enantioselective arylation of aromatic aldehydes.

机构信息

State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin, People's Republic of China.

出版信息

Org Biomol Chem. 2021 Apr 28;19(16):3644-3655. doi: 10.1039/d1ob00289a.

Abstract

Binaphthyl-prolinol ligands were designed and applied in enantioselective arylation of aromatic aldehydes and sequential arylation-lactonization of methyl 2-formylbenzoate. Under optimized conditions, the reactions provided the desired diarylmethanols and 3-aryl phthalides in up to 96% yields with up to 99% ee and up to 89% yields with up to 99% ee, respectively. In particular, essentially optically pure 3-aryl phthalides (over 99% ee) were obtained in large quantities through recrystallization.

摘要

联萘酚脯氨酸配体被设计并应用于芳香醛的对映选择性芳基化反应和甲酯 2-甲酰苯甲酸的串联芳基化-内酯化反应。在优化条件下,这些反应以高达 96%的收率、高达 99%的对映选择性和高达 89%的收率得到所需的二芳基甲醇和 3-芳基邻苯二甲酸酐,分别。特别是,通过重结晶可以获得大量基本上光学纯的 3-芳基邻苯二甲酸酐(超过 99%的对映选择性)。

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