General approach to the synthesis of prochiral atropisomeric biaryls.

ISRN Organic Chemistry Pub Date : 2011-06-26 eCollection Date: 2011-01-01 DOI:10.5402/2011/919102
Katarzyna Kielar, Oleg M Demchuk, K Michał Pietrusiewicz
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引用次数: 3

Abstract

General approach to the synthesis of prochiral precursors of chiral atropisomeric biaryls based on several complementary methods has been developed. Biaryls were obtained in good to excellent yields depending on their structure and selected method of synthesis. Furthermore, we demonstrate a possibility of utilisation of the obtained compounds possessing 2 or 3 ortho substituents around the aryl-aryl bond in direct and directed arylation reaction leading through transition metal-mediated C-H bond activation to atropisomeric compounds.

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前手性异位体双芳基合成的一般方法。
在几种互补方法的基础上,综述了手性二芳异构的前手性前体的合成方法。根据其结构和所选择的合成方法,可以获得良好到优异的收率。此外,我们证明了利用所获得的化合物在芳基-芳基键周围具有2或3个邻位取代基的可能性,通过过渡金属介导的C-H键激活直接和定向芳基化反应生成atropisomer化合物。
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