1181455-08-2Relevant academic research and scientific papers
[Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source
Liu, Yungen,Wei, Jinhu,Che, Chi-Ming
supporting information; experimental part, p. 6926 - 6928 (2010/11/16)
The syntheses of alkaloids including indoles, indolines, tetrahydroquinolines, dihydroquinazolinones and quinazolinones have been accomplished in moderate to excellent yields via [Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation using aryl azides as nitrogen source.
Intramolecular Ir(I)-catalyzed benzylic C-H bond amination of ortho-substituted aryl azides
Sun, Ke,Sachwani, Rachna,Richert, Kathleen J.,Driver, Tom G.
supporting information; experimental part, p. 3598 - 3601 (2011/02/23)
Image Persented Iridium(I) catalyzes the intramolecular benzylic C-H bond amination of ortho-homobenzyl-substituted aryl azides to produce indolines at 25 °C.
