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JOURNALS // Mendeleev Communications // Archive

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. Trofimova, A. M. Vasil'tsova, I. A. Ushakova, A. V. Ivanova, E. Yu. Schmidta, A. I. Mikhalevaa, N. I. Protsuka, V. B. Kobychevb

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-1H-benz[g]indole on NiS/Al2O3 (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



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