Aryl amination using ligand-free Ni(II) salts and photoredox catalysis

Aryl amination using ligand-free Ni(II) salts and photoredox catalysis

Over the past two decades, there have been major developments in transition metal-catalyzed aminations of aryl halides to form anilines, a common structure found in drug agents, natural product isolates, and fine chemicals. Many of these approaches have enabled highly efficient and selective couplin...

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Bibliographic Details
Main Authors: Corcoran, Emily B., Lin, Shishi, Dreher, Spencer D., DiRocco, Daniel A., Davies, Ian W., MacMillan, David W. C., Pirnot, Michael T, Buchwald, Stephen Leffler
Other Authors: Massachusetts Institute of Technology. Department of Chemistry
Format: Article
Published: American Association for the Advancement of Science (AAAS) 2018
Online Access:http://hdl.handle.net/1721.1/113060
https://orcid.org/0000-0002-7896-1683
https://orcid.org/0000-0003-3875-4775

Internet

http://hdl.handle.net/1721.1/113060
https://orcid.org/0000-0002-7896-1683
https://orcid.org/0000-0003-3875-4775

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