Silver-Mediated Fluorination of Functionalized Aryl Stannanes

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Silver-Mediated Fluorination of Functionalized Aryl Stannanes

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Title: Silver-Mediated Fluorination of Functionalized Aryl Stannanes
Author: Ritter, Tobias; Furuya, Takeru; Strom, Alexandra E.

Note: Order does not necessarily reflect citation order of authors.

Citation: Furuya, Takeru, Alexandra E. Strom, and Tobias Ritter. 2009. Silver-mediated fluorination of functionalized aryl stannanes. Journal of the American Chemical Society 131(5): 1662-1663.
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Abstract: We report a regiospecific silver-mediated fluorination of aryl stannanes. The presented reaction can afford complex fluoroarenes from readily available phenols in three steps. The operational simplicity and the broad substrate scope of the fluorination should render this reaction a useful tool for the synthesis of milligram to gram quantities of functionalized aryl fluorides. Silver-mediated oxidative transformations of aryl nucleophiles that proceed via bimetallic redox processes are a new avenue to develop carbon−heteroatom bond formations.
Published Version: doi:10.1021/ja8086664
Other Sources: http://www.ncbi.nlm.nih.gov/pubmed/19191693
Terms of Use: This article is made available under the terms and conditions applicable to Open Access Policy Articles, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#OAP
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:8156524
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