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首页> 外文期刊>Angewandte Chemie >Highly Enantioselective Synthesis of Axially Chiral Biarylphosphonates: Asymmetric Suzuki-Miyaura Coupling Using High-Molecular-Weight, Helically Chiral Polyquinoxaline-Based Phosphines
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Highly Enantioselective Synthesis of Axially Chiral Biarylphosphonates: Asymmetric Suzuki-Miyaura Coupling Using High-Molecular-Weight, Helically Chiral Polyquinoxaline-Based Phosphines

机译:轴向手性联芳基膦酸酯的高对映选择性合成:使用高分子量,螺旋手性聚喹喔啉基膦的不对称Suzuki-Miyaura偶联

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摘要

Asymmetric synthesis has developed rapidly with the exploration of chiral molecular scaffolds for use as chiral ligands, reagents, and auxiliaries. Some molecular frameworks such as 1,1'-binaphthyl are widely recognized as privileged scaffolds for chiral sciences and technologies, including not only asymmetric synthesis, but also chiral recognition and separa-tion. In addition to those small-molecule-based chiral scaffolds for asymmetric synthesis, recent efforts have also been devoted to the development of macromolecular chiral scaffolds for asymmetric synthesis.
机译:随着探索用作手性配体,试剂和助剂的手性分子支架,不对称合成得到了迅速发展。一些分子骨架,例如1,1'-联萘已被广泛认为是手性科学和技术的特权支架,不仅包括不对称合成,还包括手性识别和分离。除了那些用于不对称合成的基于小分子的手性支架外,最近还致力于开发用于不对称合成的大分子手性支架。

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