首页> 外文期刊>Doklady Chemistry >Palladium-Catalyzed Reactions of Halogen Derivatives of N,N- Dimethyl- 1-Phenylethanamine with Arylboronic Acids as a Novel Approach to the Synthesis of Biaryls with Central and Axial Chirality
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Palladium-Catalyzed Reactions of Halogen Derivatives of N,N- Dimethyl- 1-Phenylethanamine with Arylboronic Acids as a Novel Approach to the Synthesis of Biaryls with Central and Axial Chirality

机译:N,N-二甲基-1-苯基乙胺的卤素衍生物与芳基硼酸的钯催化反应是合成具有中心和轴向手性的芳基的新方法

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摘要

Biaryls with axial chirality (atropoisomerism), which appears due to hindered rotation around the Ar-Ar bonds in the presence of at least one bulky sub-stituent in the ortho-position, occur as structural units in some natural molecules . Examples of these compounds are the antibiotic vancomycin , the antitumor lignan steganacin , and the anti-HIV agent Michelamine B. Furthermore, biaryl derivatives with axial chirality are widely used in the catalytic asymmetric synthesis as efficient ligands.
机译:在某些天然分子中,由于存在至少一个大的取代基而导致在Ar-Ar键周围旋转受阻而出现的具有轴向手性的手性芳基芳烃(对映异构)。这些化合物的例子是抗生素万古霉素,抗肿瘤木脂体甜菊糖和抗HIV试剂MichelamineB。此外,具有轴向手性的联芳基衍生物广泛用作催化不对称合成中的有效配体。

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