Ligated Pd-Catalyzed Aminations of Aryl/Heteroaryl Halides with Aliphatic Amines under Sustainable Aqueous Micellar Conditions

Ligated Pd-Catalyzed Aminations of Aryl/Heteroaryl Halides with Aliphatic Amines under Sustainable Aqueous Micellar Conditions
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DOI:
10.1021/jacsau.3c00742
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发表时间:
2024-02-12
期刊:
影响因子:
8
通讯作者:
Lipshutz,Bruce H.
Lipshutz,Bruce H.
中科院分区:
其他
文献类型:
--
作者:
Iyer,Karthik S.;Kavthe,Rahul D.;Lipshutz,Bruce H.

文献摘要

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报道了一种可持续的技术,用于构建Pd催化的脂肪胺C-N键。一个催化系统,依赖于低水平的可回收的贵金属,一个已知的和商业上可获得的配体,和一个可回收的水介质相结合,导致一个新开发的程序。这项新技术可以在海水中使用,同样有效。涉及构成后期官能化的高度挑战性的反应伙伴的应用被记录,因为是药物萘哌地尔的短而有效的合成。与现有胺化的比较突出了所提供的许多进步。
Sustainable technology for constructing Pd-catalyzed C–N bonds involving aliphatic amines is reported. A catalytic system that relies onlow levels of recyclable precious metal, a known andcommercially available ligand, and arecyclable aqueous mediumare combined, leading to a newly developed procedure. This new technology can be used in ocean water with equal effectiveness. Applications involving highly challenging reaction partners constituting late-stage functionalization are documented, as is a short but efficient synthesis of the drug naftopidil. Comparisons with existing aminations highlight the many advances being offered.