187272-07-7Relevant academic research and scientific papers
Synthesis of an indole analog of magallanesine via the [1,2]-Meisenheimer rearrangement
Yoneda, Ryuji,Kimura, Tetsuya,Kinomoto, Junko,Harusawa, Shinya,Kurihara, Takushi
, p. 1909 - 1913 (2007/10/03)
Ring expansion of azetopyridoindole 11 via the [1,2]-Meisenheimer rearrangement of the corresponding N-oxide 12 gave azocinoindole 14, which was converted into the N-benzoylenaminone 18 in 5 steps. Intramolecular cyclization of 18 was accomplished by a mo
