首页> 外文期刊>Chirality: The pharmacological, biological, and chemical consequences of molecular asymmetry >A Helical Polyphenylacetylene Having Amino Alcohol Moieties Without Chiral Side Groups as a Chiral Ligand for the Asymmetric Addition of Diethylzinc to Benzaldehyde
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A Helical Polyphenylacetylene Having Amino Alcohol Moieties Without Chiral Side Groups as a Chiral Ligand for the Asymmetric Addition of Diethylzinc to Benzaldehyde

机译:具有不带手性侧基的氨基醇部分作为手性配体的螺旋聚苯乙炔,用于将二乙基锌不对称加成到苯甲醛中

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摘要

One-handed helical polyphenylacetylenes having achiral amino alcohol moieties, but no chiral side groups, were synthesized by the helix-sense-selective copolymerization of an achiral phenylacetylene having an amino alcohol side group with a phenylacetylene having two hydroxyl groups. Since the resulting helical copolymers were successfully utilized as chiral ligands for the enantioselective alkylation of benzaldehyde with diethylzinc, we can conclude that the main-chain chirality based on the one-handed helical conformation is useful for the chiral catalysis of an asymmetric reaction for the first time. The enantioselectivities of the reaction were controlled by the optical purities of the helical polymer ligands. In addition, the polymer ligands could be easily recovered by precipitation after the reaction. Chirality 27:454-458, 2015. (c) 2015 Wiley Periodicals, Inc.
机译:通过具有氨基醇侧基的非手性苯基乙炔与具有两个羟基的苯基乙炔的螺旋-感觉-选择性共聚,合成具有非手性氨基醇基团但没有手性侧基的单手螺旋聚苯基乙炔。由于所得的螺旋共聚物已成功地用作苯甲醛与二乙基锌的对映选择性烷基化的手性配体,因此我们可以得出结论,基于单手螺旋构象的主链手性可用于手性催化第一个不对称反应时间。反应的对映选择性由螺旋聚合物配体的光学纯度控制。另外,反应后通过沉淀可以容易地回收聚合物配体。手性27:454-458,2015.(c)2015 Wiley Periodicals,Inc.

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