Abstract
Reductive cross-coupling allows the direct C-C bond formation between two organic halides without the need for preformation of an organometallic reagent. A method has been developed for the reductive cross-coupling of nonaromatic, heterocyclic bromides with aryl or heteroaryl bromides. The developed conditions use an air-stable Ni(II) source in the presence of a diamine ligand and a metal reductant to allow late-stage incorporation of saturated heterocyclic rings onto aryl halides in a functional-group tolerant manner. © 2014 American Chemical Society.
Cite
CITATION STYLE
Molander, G. A., Traister, K. M., & ONeill, B. T. (2014). Reductive cross-coupling of nonaromatic, heterocyclic bromides with aryl and heteroaryl bromides. Journal of Organic Chemistry, 79(12), 5771–5780. https://doi.org/10.1021/jo500905m
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.