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Nickel-catalyzed 1,2-phenyl migrations of 3-Azidoindolin-2-ones | Synapse
March 3, 2026
Nickel-catalyzed 1,2-phenyl migrations of 3-Azidoindolin-2-ones
GL
Gongmei Luo
KW
Kai Wang
TY
Tonghao Yang
Guizhou Minzu University
Key Points
1,2-phenyl migrations occur effectively with nickel as the catalyst, showcasing high efficiency and selectivity.
The presence of azidoindolin-2-ones enables diverse transformations, expanding synthetic inroads for complex molecules.
Utilization of nickel-based catalysis presents a green alternative to traditional methods while minimizing environmental impact.
While this approach showcases promising results, further optimization and exploration of reaction conditions are necessary.
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Luo et al. (Fri,) studied this question.
synapsesocial.com/papers/69a76801badf0bb9e87e3391
https://doi.org/https://doi.org/10.1016/j.tetlet.2026.155996
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