Abstract
A wide variety of bench-stable potassium heteroaryltrifluoroborates were prepared, and general reaction conditions were developed for their cross-coupling to aryl and heteroaryl halides. The cross-coupled products were obtained in good to excellent yields. This method represents an efficient and facile installation of heterocyclic building blocks onto preexisting organic substructures. © 2009 American Chemical Society.
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CITATION STYLE
Molander, G. A., Canturk, B., & Kennedy, L. E. (2009). Scope of the suzuki-Miyaura cross-coupling reactions of potassium heteroaryltrifluoroborates. Journal of Organic Chemistry, 74(3), 973–980. https://doi.org/10.1021/jo802590b
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