186586-76-5Relevant academic research and scientific papers
Metal-catalyzed reactions between 2-azabicyclo[2.2.1]hept-5-en-3-ones and arylboronic acids
Abe, Takumi,Takeda, Hiroyuki,Takahashi, Yumi,Miwa, Yoshihisa,Yamada, Koji,Ishikura, Minora
experimental part, p. 3281 - 3294 (2010/09/05)
Cu- and Rh-catalyzed coupling reactions of 2-azabicyclo[2.2.1]hept-5-en-3- ones (1) with arylboronic acids were successful carried out under microwave irradiation conditions and yielded N-aryl and C-aryl derivatives of 1, respectively.
New N- and O-arylations with phenylboronic acids and cupric acetate
Chan, Dominic M. T.,Monaco, Kevin L.,Wang, Ru-Ping,Winters, Michael P.
, p. 2933 - 2936 (2007/10/03)
A new method of arylating N-H and O-H containing compounds at room temperature with phenylboronic acids and cupric acetate in the presence of a tertiary amine promoter is described. Substrates include phenols, amines, anilines, amides, imides, ureas, carbamates, and sulfonamides.
Promotion of reaction of N-H bonds with triarylbismuth and cupric acetate
Chan, Dominic M. T.
, p. 9013 - 9016 (2007/10/03)
Arylation of a diverse group of N-H containing compounds at room temperature with triarylbismuth and cupric acetate in the presence of a tertiary amine promoter, such as triethylamine or pyridine, is described. This mild and highly efficient procedure, which is based on Barton's earlier work on the arylation of amines, can be applied to amides, imides, ureas, carbamates, and sulfonamides. Copyright (C) 1996 Elsevier Science Ltd.
