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可拉伸手性口袋用于钯催化的高化学选择性和对映选择性烯丙基化反应。

Stretchable chiral pockets for palladium-catalyzed highly chemo- and enantioselective allenylation.

机构信息

Laboratory of Molecular Recognition and Synthesis, Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang, P. R. China.

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, P. R. China.

出版信息

Nat Commun. 2021 Apr 23;12(1):2416. doi: 10.1038/s41467-021-22498-1.

Abstract

Pyrazolones are a vital class of heterocycles possessing various biological properties and much attention is paid to the diversified synthesis of enantiopure pyrazolone derivatives. We describe here the development of diphenylphosphinoalkanoic acid based chiral bisphosphine ligands, which are successfully applied to the palladium-catalyzed asymmetric allenylation of racemic pyrazol-5-ones. The reaction affords C-allenylation products, optically active pyrazol-5-ones bearing an allene unit, in high chemo- and enantioselectivity, with DACH-ZYC-Phos-C1 as the best ligand. The synthetic potential of the C-allenylation products is demonstrated. Furthermore, the enantioselectivity observed with DACH-ZYC-Phos-C1 is rationalized by density functional theory studies.

摘要

吡唑酮是一类重要的杂环化合物,具有多种生物活性,因此人们对其手性吡唑酮衍生物的多样化合成给予了高度关注。在这里,我们描述了基于二苯基膦基烷酸的手性双膦配体的开发,该配体成功应用于外消旋吡唑-5-酮的钯催化不对称烯丙基化反应中。该反应以高化学选择性和对映选择性得到了 C-烯丙基化产物,即具有丙二烯单元的光学活性吡唑-5-酮,其中 DACH-ZYC-Phos-C1 是最好的配体。展示了 C-烯丙基化产物的合成潜力。此外,通过密度泛函理论研究对 DACH-ZYC-Phos-C1 观察到的对映选择性进行了合理化解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7550/8065118/695ad4bca4cd/41467_2021_22498_Fig1_HTML.jpg

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