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Bischler-Möhlau indole synthesis

  • Jie Jack Li

Abstract

Heating excess of aniline with 2-bromo-1-phenyl-ethanone to afford 2-arylindoles.

Keywords

Inorganic Chemistry Organic Chemistry Heating Excess Addition Elimination Synthesis Heating 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

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    Möhlau, R. Ber. Dtsch. Chem. Ges. 1881, 14, 171.CrossRefGoogle Scholar
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    Sundberg, R. J. The Chemistry of Indoles Academic Press: New York, 1970, p 164. (Review).Google Scholar
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    Buu-Hoï, N. P.; Saint-Ruf, G.; Deschamps, D.; Bigot, P. J. Chem. Soc. (C) 1971, 2606.Google Scholar
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    The Chemistry of Heterocycl. Compounds, Indoles (Part 1), Houlihan, W. J., ed.; Wiley & Sons: New York, 1972. ( Review).Google Scholar
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    Bancroft, K. C. C.; Ward, T. J. J. Chem. Soc., Perkin 1 1974, 1852.CrossRefGoogle Scholar
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    Coic, J. P.; Saint-Ruf, G. J. Heterocycl. Chem. 1978, 15, 1367.Google Scholar
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    Henry, J. R.; Dodd, J. H. Tetrahedron Lett. 1998, 39, 8763.CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2003

Authors and Affiliations

  • Jie Jack Li
    • 1
  1. 1.Chemistry DepartmentPfizer Global Research and DevelopmentAnn ArborUSA

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