Nickel-Catalyzed Synthesis of Primary Aryl and Heteroaryl Amines via C–O Bond Cleavage

Huifeng Yue, Lin Guo, Xiangqian Liu, Magnus Rueping

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

A nickel-catalyzed protocol for the conversion of aryl and heteroaryl alcohol derivatives to primary and secondary aromatic amines via C(sp2)-O bond cleavage is described. The new amination protocol can be applied to a range of substrates bearing diverse functional groups and uses readily available benzophenone imines as an effective nitrogen source.
Original languageEnglish (US)
Pages (from-to)1788-1791
Number of pages4
JournalOrganic Letters
Volume19
Issue number7
DOIs
StatePublished - Mar 13 2017

Fingerprint Dive into the research topics of 'Nickel-Catalyzed Synthesis of Primary Aryl and Heteroaryl Amines via C–O Bond Cleavage'. Together they form a unique fingerprint.

Cite this