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Remote site-selective C–H activation directed by a catalytic bifunctional template

Converting C–H bonds directly into carbon-carbon and carbon-heteroatom bonds can significantly improve step-economy in synthesis by providing alternative disconnections to traditional functional group manipulations. In this context, directed C–H activation reactions have been extensively explored fo...

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Podrobná bibliografie
Vydáno v:Nature
Hlavní autoři: Zhang, Zhipeng, Tanaka, Keita, Yu, Jin-Quan
Médium: Artigo
Jazyk:Inglês
Vydáno: 2017
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5477648/
https://ncbi.nlm.nih.gov/pubmed/28273068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature21418
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