Synthetic communications

Facile Synthesis of 2-Benzylindoles

P Wiedenau, S Blechert

Index: Wiedenau, Paul; Blechert, Siegfried Synthetic Communications, 1997 , vol. 27, # 12 p. 2033 - 2039

Full Text: HTML

Citation Number: 16

Abstract

The indole nucleus is common to a large number of biologically active natural and synthetic compounds.' Their structural diversity and broad spectrum of pharmacological properties have attracted considerable attention in medicinal chemistry.* The particular interest for indoles substituted in the 2-position3 and the limited availability of synthetic routes4 towards them ... T o whom correspondence should be addressed ... We found, that the benzyl group of N-benzylindole 1 migrates ...

Related Articles:

Rapid and General Protocol towards Catalyst??Free Friedel–Crafts C??Alkylation of Indoles in Water Assisted by Microwave Irradiation

[De Rosa, Margherita; Soriente, Annunziata European Journal of Organic Chemistry, 2010 , # 6 p. 1029 - 1032]

One-pot synthesis of polysubstituted indoles from aliphatic nitro compounds under mild conditions

[Simoneau, Christopher A.; Strohl, Alexis M.; Ganem, Bruce Tetrahedron Letters, 2007 , vol. 48, # 10 p. 1809 - 1811]

Zeolites as catalysts in the Fischer indole synthesis. Enhanced regioselectivity for unsymmetrical ketone substrates

[Prochazka, Michal P.; Eklund, Lars; Carlson, Rolf Acta Chemica Scandinavica, 1990 , vol. 44, # 6 p. 610 - 613]

More Articles...