Issue 8, 1977

Competition between single electron transfer and nucleophilic attack: reaction of 3-arylimino-2-phenyl-3H-indoles with organolithium compounds

Abstract

3-Arylimino-2-phenyl-3H-indoles react with organo-lithium compounds giving 1,2-addition, 1,4-addition, and reduction products; the extents of formation of these compounds depend on the substituent para with respect to the arylimino-group. Competition between single electron transfer and nucleophilic attack is discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1977, 1032-1035

Competition between single electron transfer and nucleophilic attack: reaction of 3-arylimino-2-phenyl-3H-indoles with organolithium compounds

C. Berti, L. Greci and L. Marchetti, J. Chem. Soc., Perkin Trans. 2, 1977, 1032 DOI: 10.1039/P29770001032

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