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• W2163655706 startingPage "11677" @default.
• W2163655706 abstract "The first example of a transition-metal-catalyzed, meta-selective CH bromination procedure is reported. In the presence of catalytic [{Ru(p-cymene)Cl2}2], tetrabutylammonium tribromide can be used to functionalize the meta CH bond of 2-phenylpyridine derivatives, thus affording difficult to access products which are highly predisposed to further derivatization. We demonstrate this utility with one-pot bromination/arylation and bromination/alkenylation procedures to deliver meta-arylated and meta-alkenylated products, respectively, in a single step." @default.
• W2163655706 created "2016-06-24" @default.
• W2163655706 creator A5009682819 @default.
• W2163655706 creator A5011010570 @default.
• W2163655706 creator A5083780663 @default.
• W2163655706 date "2015-08-18" @default.
• W2163655706 modified "2023-09-29" @default.
• W2163655706 title "Ruthenium‐Catalyzed <i>meta</i> ‐Selective CH Bromination" @default.
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• W2163655706 doi "https://doi.org/10.1002/anie.201504390" @default.
• W2163655706 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4678425" @default.
• W2163655706 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26288217" @default.
• W2163655706 hasPublicationYear "2015" @default.
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