1187159-22-3Relevant academic research and scientific papers
Zinc-mediated highly α-regioselective prenylation of imines with prenyl bromide
Zhao, Li-Ming,Zhang, Shu-Qing,Jin, Hai-Shan,Wan, Li-Jing,Dou, Fei
supporting information; experimental part, p. 886 - 889 (2012/04/17)
A highly α-regioselective prenylation of imines has been successfully developed. The efficiency of this approach is confirmed by a wide range of imines including N- and C-aryl aldimines, N-alkyl aldimines, C-alkyl aldimines, and N- and C-aryl ketimines. T
Generation of prenylhafnlum and α-selectlve addition to imines
Shibata, Ikuya,Miyamoto, Shinji,Tsunoi, Shinji,Sakamoto, Kazuya,Baba, Akio
experimental part, p. 3508 - 3511 (2009/12/01)
Allylhafnium compounds were generated by transmetalation between allyl-SnBu3 and HfCl4 in EtCN. A highly α-selective addition reaction of prenyltributyltin to imines was observed.
