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手性酰胺导向的非对映和对映纯超分子主体的组装及其在手性中性底物对映选择性催化中的应用。

Chiral amide directed assembly of a diastereo- and enantiopure supramolecular host and its application to enantioselective catalysis of neutral substrates.

机构信息

Chemical Sciences Division, Lawrence Berkeley National Laboratory, and Department of Chemistry, University of California , Berkeley, California 94720, United States.

出版信息

J Am Chem Soc. 2013 Dec 18;135(50):18802-5. doi: 10.1021/ja411631v. Epub 2013 Dec 5.

DOI:10.1021/ja411631v
PMID:24283463
Abstract

The synthesis of a novel supramolecular tetrahedral assembly of K12Ga4L6 stoichiometry is reported. The newly designed chiral ligand exhibits high diastereoselective control during cluster formation, leading exclusively to a single diastereomer of the desired host. This new assembly also exhibits high stability toward oxidation or a low pH environment and is a more robust and efficient catalyst for asymmetric organic transformations of neutral substrates.

摘要

本文报道了一种新型超分子四面体 K12Ga4L6 配合物的合成。新设计的手性配体在形成簇时表现出高的非对映选择性控制,仅得到所需主体的单一非对映异构体。这种新的组装体对氧化或低 pH 环境也表现出高的稳定性,并且是更有效的不对称有机转化的中性底物的催化剂。

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