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金(I)催化的 1,3-二取代烯丙基与高效轴向到点手性转移的芳基化反应。

Gold(I)-Catalysed Hydroarylation of 1,3-Disubstituted Allenes with Efficient Axial-to-Point Chirality Transfer.

机构信息

Institute of Chemical Sciences, School of Engineering and Physical Sciences, Heriot-Watt University, Edinburgh, EH14 4AS, UK.

出版信息

Chemistry. 2018 May 11;24(27):7002-7009. doi: 10.1002/chem.201800209. Epub 2018 Apr 26.

Abstract

Hydroarylation of enantioenriched 1,3-disubstituted allenes has the potential to proceed with axial-to-point chirality transfer to yield enantioenriched allylated (hetero)aryl compounds. However, the gold-catalysed intermolecular reaction was previously reported to occur with no chirality transfer owing to competing allene racemisation. Herein, we describe the development of the first intermolecular hydroarylations of allenes to proceed with efficient chirality transfer and summarise some of the key criteria for achieving high regio- and stereoselectivity.

摘要

对映富集的 1,3-二取代丙二烯的氢芳基化反应具有通过轴向到点的手性转移来生成对映富集的烯丙基化(杂)芳基化合物的潜力。然而,先前报道的金催化的分子间反应由于丙二烯的外消旋化而没有发生手性转移。在此,我们描述了首例丙二烯的分子间氢芳基化反应,该反应具有高效的手性转移,并总结了实现高区域和立体选择性的一些关键标准。

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