Cover Feature: Nickel‐Catalyzed Synthesis of Diaryl Sulfones from Aryl Halides and Sodium Sulfinates (Eur. J. Org. Chem. 10/2018)

Cover Feature: Nickel‐Catalyzed Synthesis of Diaryl Sulfones from Aryl Halides and Sodium... The Cover Feature shows the first nickel‐catalyzed cross‐coupling of sodium sulfinates with aryl bromides. This method enables a straightforward synthesis of diarylsulfones with high functional group compatibility. The active nickel‐catalyst is generated in situ from the nickel(II) precursor NiBr2, an N‐heterocyclic carbene ligand, and triethylsilane as reducing agent. More information can be found in the Communication by G. Manolikakes et al. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png European Journal of Organic Chemistry Wiley

Cover Feature: Nickel‐Catalyzed Synthesis of Diaryl Sulfones from Aryl Halides and Sodium Sulfinates (Eur. J. Org. Chem. 10/2018)

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Publisher
Wiley Subscription Services, Inc., A Wiley Company
Copyright
© 2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
ISSN
1434-193X
eISSN
1099-0690
D.O.I.
10.1002/ejoc.201800174
Publisher site
See Article on Publisher Site

Abstract

The Cover Feature shows the first nickel‐catalyzed cross‐coupling of sodium sulfinates with aryl bromides. This method enables a straightforward synthesis of diarylsulfones with high functional group compatibility. The active nickel‐catalyst is generated in situ from the nickel(II) precursor NiBr2, an N‐heterocyclic carbene ligand, and triethylsilane as reducing agent. More information can be found in the Communication by G. Manolikakes et al.

Journal

European Journal of Organic ChemistryWiley

Published: Jan 14, 2018

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