Nickel-Catalyzed Synthesis of Primary Aryl and Heteroaryl Amines via C–O Bond Cleavage
Type
Article
KAUST Department
Physical Sciences and Engineering (PSE) DivisionChemical Science Program
KAUST Catalysis Center (KCC)
Date
2017-03-13Permanent link to this record
http://hdl.handle.net/10754/623870Metadata
Show full item recordAbstract
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.Citation
Yue H, Guo L, Liu X, Rueping M (2017) Nickel-Catalyzed Synthesis of Primary Aryl and Heteroaryl Amines via C–O Bond Cleavage. Organic Letters 19: 1788–1791. Available: http://dx.doi.org/10.1021/acs.orglett.7b00556.Sponsors
H.Y., L.G., and X.L. were supported by the China Scholarship Council. Financial support by KAUST is gratefully acknowledged.Publisher
American Chemical Society (ACS)Journal
Organic LettersISSN
1523-70601523-7052