1309752-04-2Relevant academic research and scientific papers
Rhodium(III)-Catalyzed Oxidative ortho-Olefination of Phenyl Carbamates with Alkenes: Elucidation of Acceleration Mechanisms by Using an Unsubstituted Cyclopentadienyl Ligand
Tanaka, Jin,Nagashima, Yuki,Tanaka, Ken
supporting information, p. 7181 - 7186 (2020/09/02)
It has been established that an unsubstituted cyclopentadienyl (Cp) Rh(III) complex is an effective catalyst for the oxidative ortho-olefination of phenyl carbamates with both acrylates and styrenes under mild conditions. In addition, diolefination of a p
Ruthenium-catalyzed oxidative C-H alkenylation of aryl carbamates
Li, Jie,Kornhaass, Christoph,Ackermann, Lutz
supporting information, p. 11343 - 11345,3 (2012/12/12)
A cationic ruthenium(ii) catalyst enabled highly efficient oxidative alkenylations of electron-rich arenes bearing removable, weakly coordinating carbamates, and allowed for cross-dehydrogenative C-H bond functionalization in an aerobic manner. This journ
Rhodium-catalyzed selective C-H activation/olefination of phenol carbamates
Gong, Tian-Jun,Xiao, Bin,Liu, Zhao-Jing,Wan, Jian,Xu, Jun,Luo, Dong-Fen,Fu, Yao,Liu, Lei
supporting information; experimental part, p. 3235 - 3237 (2011/08/22)
Rh(III)-catalyzed ortho C-H activation/olefination of phenol carbamates has been developed. High regioselectivity is observed with a range of phenol carbamates enabling efficient coupling with acrylates and styrenes. This reaction exhibits different react
