1201594-21-9Relevant articles and documents
Nickel-catalyzed amination of aryl sulfamates
Ramgren, Stephen D.,Silberstein, Amanda L.,Yang, Yang,Garg, Neil K.
, p. 2171 - 2173 (2011/04/25)
Broad in scope: The first amination of aryl sulfamates, which are attractive cross-coupling partners, particularly for multistep syntheses, was achieved by using a nickel catalyst. The method provides a versatile means to use simple derivatives of phenol as precursors to polysubstituted aryl amines, as exemplified by a concise synthesis of the antibacterial drug linezolid (see scheme).
Suzuki-Miyaura coupling of aryl carbamates, carbonates, and sulfamates
Quasdorf, Kyle W.,Riener, Michelle,Petrova, Krastina V.,Garg, Neil K.
supporting information; experimental part, p. 17748 - 17749 (2010/04/01)
(Chemical Equation Presented) The first Suzuki-Miyaura cross-couplings of carbamates, carbonates, and sulfamates is described. The method provides a powerful means of using simple derivatives of phenol as precursors to polysubstituted aromatic compounds, as exemplified by a concise synthesis of the anti-inflammatory drug flurbiprofen.
