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首页> 外文期刊>Journal of the American Chemical Society >Synthesis of Isomerically Pure (Z)-Alkenes from Terminal Alkynes and Terminal Alkenes: Silver-Catalyzed Hydroalkylation of Alkynes
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Synthesis of Isomerically Pure (Z)-Alkenes from Terminal Alkynes and Terminal Alkenes: Silver-Catalyzed Hydroalkylation of Alkynes

机译:从末端炔烃和末端烯烃合成异构纯(Z)-烯烃:银催化的炔烃加氢烷基化

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摘要

Alkenes are an important class of compounds common among biologically active molecules and often are used as intermediates in organic synthesis. Many alkenes exist in two stereoisomeric forms (E and Z), which have different structures and different properties. The selective formation of the two isomers is an important synthetic goal that has long inspired the development of new synthetic methods. However, the efficient synthesis of diastereopure, thermodynamically less stable, Z-alkenes is still challenging. Here, we demonstrate an efficient synthesis of diastereopure Z-alkenes (Z:E > 300:1) through a silver-catalyzed hydroalkylation of terminal alkynes, using alkylboranes as coupling partners. We also describe the exploration of the substrate scope, which reveals the broad functional group compatibility of the new method. Preliminary mechanistic studies suggest that a 1,2-metalate rearrangement of the silver borate intermediate is the key step responsible for the stereochemical outcome of the reaction.
机译:烯烃是生物活性分子中常见的重要一类化合物,通常用作有机合成的中间体。许多烯烃以两种立体异构形式(E和Z)存在,具有不同的结构和不同的性质。两种异构体的选择性形成是一个重要的合成目标,长期以来一直在激发新合成方法的发展。然而,热力学上不稳定的非对映体纯的Z-烯烃的有效合成仍然具有挑战性。在这里,我们证明了通过烷基末端硼烷的银催化加氢烷基化,使用烷基硼烷作为偶联伙伴,可以高效合成非对映纯Z-烯烃(Z:E> 300:1)。我们还描述了底物范围的探索,揭示了新方法的广泛的官能团相容性。初步的机理研究表明,硼酸银中间体的1,2-金属盐重排是负责反应立体化学结果的关键步骤。

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