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Direct Amination of Unreactive C-H Bonds Catalyzed by N-hydroxyphthalimide
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Kexian Chen, Pengfei Zhang, and Prof. Haoran Li.
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Zhejiang University, China ; Oak Ridge National Laboratory, USA
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Zhejiang University, Hangzhou 310027, P.R. China ; Oak Ridge National Laboratory, Oak Ridge, Tennessee USA.
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lihr@zju.edu.cn
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The selectively direct heteratom-functionalization ofunreactive C-H bonds of readily available organic substrates (e.g. methane [1]) or complex macromolecules via simplified synthetic routes under mildconditions is of crucial importance in the academic and industrial areas, whichis a research hotspot at present and in furture. In particular,economic-friendly standards [2] require reagents, products, and conditions insuch reactions to be capable of low environmental impact, namely green enough.Compared to conventional C-H transformation protocols, recently developedinnovative Nhydroxyphthalimide (NHPI)-based catalytic systems by Ishii et al.[3-5] received great attentions [3-8] due to its environmental benign characterand established desired high reactivity.
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