88014-57-7Relevant academic research and scientific papers
Copper-catalyzed C-H oxidation/cross-coupling of α-amino carbonyl compounds
Wu, Ji-Cheng,Song, Ren-Jie,Wang, Zhi-Qiang,Huang, Xiao-Cheng,Xie, Ye-Xiang,Li, Jin-Heng
supporting information; experimental part, p. 3453 - 3457 (2012/06/01)
Keeping options open: The new and mild title reaction involving indoles selectively furnishes 1 and 2 with the aid of tert-butyl hydroperoxide (TBHP). The method represents the first example of a copper-catalyzed α arylation of α-amino carbonyl substrates leading to α-aryl α-imino and α-aryl α-oxo carbonyl compounds using a C-H oxidation strategy. Copyright
1,3-DIPOLAR CYCLOADDITIONS OF C-BENZOYL-N-PHENYLNITRONE INDOLE DERIVATIVES
Fisera, Lubor,Mesko, Peter,Lesko, Jan,Dandarova, Miloslava,Kovac, Jaroslav,Goljer, Igor
, p. 1854 - 1863 (2007/10/02)
Reaction of the title nitrone I with indole derivatives IIa,b gives the 1,3-addition product IIIa,b, its hydrogenated derivative IVa,b, and dehydrogenation products VIa,b and VIIa,b from transient product of 1,3-dipolar cycloaddition (V).Indole itself onl
