Abstract
We report an asymmetric Ni-catalyzed reductive cross-coupling of aryl/heteroaryl halides with racemic α-chlorosulfones to afford enantioenriched sulfones. The reaction tolerates a variety of functional groups under mild reaction conditions, which complements the current methods. The utility of this work was demonstrated by facile late-stage functionalization of commercial drugs.
Cite
CITATION STYLE
APA
Sun, D., Ma, G., Zhao, X., Lei, C., & Gong, H. (2021). Nickel-catalyzed asymmetric reductive arylation of α-chlorosulfones with aryl halides. Chemical Science, 12(14), 5253–5258. https://doi.org/10.1039/d1sc00283j
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free