锰催化C2烯丙化和水中吲哚的氘化

Si Lok Ko , Eimear Courtney , Dr Mark Light , Dr David Jones , Dr Gerard P. McGlacken
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引用次数: 0

摘要

Mn催化的C–H活化已成为形成新的C–C键的一种有用的可持续方法。迄今为止,大多数方案都是在有机溶剂中描述的。另一方面,水作为溶剂是非常有利的,但通常与有机金属化学不相容。在此,我们描述了在水中使用未改性的市售锰催化剂对吲哚的C–H活化。可以添加两种类型的有价值的烯丙基,并描述了良好的底物范围。C-3组的替代是可以容忍的,允许获得医学上重要的框架,反应在克级上进行。最后,利用水作为反应介质的耐受性,D2O可以用作吲哚C-2标记的廉价氘源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Manganese-catalysed C2 allylation and deuteration of indoles in water

Mn-catalysed C–H activation has emerged as a useful sustainable methodology for the formation of new C–C bonds. To date most of the protocols are described in organic solvents. Water as solvent, on the other hand, would be highly advantageous, but is often incompatible with organometallic chemistry. Herein, we describe the C–H activation of indoles using an unmodified, commercially available manganese catalyst in water. Two types of valuable allyl groups can be added and a good substrate scope is described. Substitution at the C-3 group is tolerated, allowing access to medicinally important frameworks, and the reaction works on a gram scale. Finally, harnessing the tolerance of water as the reaction medium, D2O can be used as an inexpensive source of deuterium for the C-2 labelling of indoles.

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