Mendeleev Commun., 2007 Volume 17, Issue 5, Pages 296–298
(Mi mendc3464)
This article is cited in
8 papers
A peculiar selective rearrangement during the NiS-catalysed dehydrogenation of 4,5-dihydro-1H -benz[g ]indole
B. A. Trofimov a ,
A. M. Vasil'tsov a ,
I. A. Ushakov a ,
A. V. Ivanov a ,
E. Yu. Schmidt a ,
A. I. Mikhaleva a ,
N. I. Protsuk a ,
V. B. Kobychev b a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b Irkutsk State University, Irkutsk, Russian Federation
Abstract:
The dehydrogenation of 4,5-dihydro-1
H -benz[g]indole on NiS/Al
2 O
3 (350°C) is accompanied by a peculiar rearrangement to give 3H-benz[e]indole (71%).
Language: English
DOI:
10.1016/j.mencom.2007.09.017
© , 2025