141311-38-8Relevant articles and documents
Aromatic borylation/amidation/oxidation: A rapid route to 5-substituted 3-amidophenols
Shi, Feng,Smith III, Milton R.,Maleczka Jr., Robert E.
, p. 1411 - 1414 (2006)
5-Substituted 3-amidophenols are prepared by subjecting 3-substituted halobenzenes to an Ir-catalyzed aromatic borylation, followed by a Pd-catalyzed amidation, and finally an oxidation of the boronic ester intermediate. The entire C-H activation borylation/amidation/oxidation sequence can be accomplished without isolation of any intermediate arenes. Usefully, amide partners can include lactams, carbamates, and ureas.