Issue 0, 1971

Carcinogenic nitrogen compounds. Part LXXII. The Möhlau–Bischler reaction as a preparative route to 2-arylindoles

Abstract

The Mohlau–Bischler cyclisation of ω-arylamino-ketones in the presence of arylamine hydrochlorides proved a convenient method for the preparation of diversely substituted 2-arylindoles, including polycyclic indoles; several are inducers of zoxazolamine hydroxylase.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 2606-2609

Carcinogenic nitrogen compounds. Part LXXII. The Möhlau–Bischler reaction as a preparative route to 2-arylindoles

N. P. Buu-Hoï, G. Saint-Ruf, D. Deschamps and H.-T. Hieu, J. Chem. Soc. C, 1971, 2606 DOI: 10.1039/J39710002606

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